Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

IYT — Predicate Candidate Screening

49 FDA 510(k) clearances under this product code; the 50 most recent screened below.

73 daysmedian FDA review time
171 days90th percentile
49clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K253942Pulmonex II Xenon System (132-503)Mirion Technologies (Capintec), Inc.2026-07-072100
K200916Patient Administration SetCyclomedica Australia Pty, Ltd.2020-09-011480
K953513XENON CIRCUITKing Systems Corp.1995-11-031000
K952223XENON GAS BREATHING CIRCUITIntertech Resources, Inc.1995-08-11910
K914747XENON CIRCUITGibeck, Inc.1992-02-271280
K913416TETLEY PATIENT ADMINISTRATION SETTetley Medical , Ltd.1991-10-28890
K912626BOLUS XENON CIRCUITVital Signs, Inc.1991-08-02500
K904684AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATIONAmici, Inc.1991-01-141520
K903805AMICI XENON ADMINISTRATION SETAmici, Inc.1991-01-141520
K903694AMICI TRU-FIT SOFT PLASTIC MOUTHPIECEAmici, Inc.1990-10-03490
K896885DISPOSABLE RESPIRTORY KIT (MP-200)Medipart Jerry Alexander1990-02-26800
K896125MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133MMedipart Jerry Alexander1990-02-011010
K896476DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELDMedipart Jerry Alexander1990-01-22700
K896475DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELDMedipart Jerry Alexander1990-01-22700
K896124MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133Medipart Jerry Alexander1990-01-22910
K881812AERO-MIST NEBULIZERCadema Medical Products, Inc.1988-07-18810
K871868VENTI-SCAN IIAtomic Products Corp.1988-04-113340
K872920AMICI KRYPTON ADMINISTRATION SYSTEM*Amici, Inc.1988-02-122000
K865107AERO-VENT AEROSOL UNITMedi Nuclear Corp., Inc.1987-10-202930
K865084AMICI XENON REBREATHING SYSTEM*Amici, Inc.1987-03-03630
K863996MODEL XE-103 XENON/MASTER IIMedi Nuclear Corp., Inc.1986-11-04210
K863778VENTICIS IICis-Us, Inc.1986-10-27310
K862792MP-066 RADIOAEROSOL KITMedipart Jerry Alexander1986-08-0190
K862794MP-070 RADIOAEROSOL KITMedipart Jerry Alexander1986-08-0190
K862791MP-30XM-IE FACE MASK AND FILTER KITMedipart Jerry Alexander1986-08-0190
K862795MP-070-M RADIOAEROSOL KITMedipart Jerry Alexander1986-08-0190
K862793MP-066-M RADIOAEROSOL KITMedipart Jerry Alexander1986-08-0190
K853576MEDIPART DISPOS. XENON 133 ADMIN. SET MP-0133MMedipart Jerry Alexander1985-11-07730
K853579MEDIPART DISPOS. XENON 133 ADMIN. SYS MP-0133Medipart Jerry Alexander1985-11-07730
K853570MEDIPART DRIERITE MP-1002Medipart Jerry Alexander1985-11-07730
K851198MEDIPART LUNG AEROSOL KIT MP-1012AMedipart Jerry Alexander1985-09-101680
K851199MEDIPART LUNG AEROSOL KIT MP-1012A-MMedipart Jerry Alexander1985-09-101680
K851200MEDIPART LUNG AEROSOL KIT MP-1024AMedipart Jerry Alexander1985-09-101680
K851201MEDIPART LUND AEROSOL KIT MP-1024A-MMedipart Jerry Alexander1985-09-101680
K850836MEDIPART FACE MASK MP-XM-IMedipart Jerry Alexander1985-08-191710
K850837MEDIPART FACE MASK & FILTER MP-30XM-IMedipart Jerry Alexander1985-08-191710
K853056RESPIR GARD-II FACE MASK CORRUGATED TUBINGMarquest Medical Products, Inc.1985-08-07190
K852693XEN-REX INuclear Pharmacy, Inc.1985-07-24280
K850367MEDIPART XENON BREATHING KIT MP-02XM-IMedipart Jerry Alexander1985-04-30900
K850366MEDIPART XENON BREATHING KIT MP-OIXM-IMedipart Jerry Alexander1985-04-30900
K843640XENON XE 127/XE 133 GAS DISPENSERMallinckrodt Critical Care1985-01-141190
K844496MEDIPART XENON BREATHING KIT MP-01XMMedipart Jerry Alexander1984-12-24340
K844495MEDIPART XENON BREATHING KIT MP-02XMMedipart Jerry Alexander1984-12-17270
K820571XENAMATIC SERIES OF XENON REBREATH DEVDiversified P.A.1982-03-31290
K820143XENON DELIVERY SYSTEMVital Signs, Inc.1982-03-02420
K811118KRYPTON MASKS & TUBINGMedi-Physics Inc. Dba Nycomed Amersham Imaging1981-06-02390
K810819MEDI/NUCLEAR #XE-102 XENON/MASTERMedi Nuclear Corp., Inc.1981-04-14210
K781933DISPENSOR, XENON GASDiagnostic Isotapes, Inc.1978-12-04140
K781107DISPENSER, GAS XENONMallinckrodt Critical Care1978-07-17170

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda