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Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

Intertech Resources, Inc. — Predicate Candidate Screening

29 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

90 daysmedian FDA review time
159 days90th percentile
29clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K9613181ST RESPONSE DISPOSABLE MANOMETERIntertech Resources, Inc.1996-12-172560
K955008HEAT & MOISTURE EXCHANGERIntertech Resources, Inc.1996-01-30900
K953580HEAT MOISTURE EXCHANGERIntertech Resources, Inc.1995-09-15450
K952223XENON GAS BREATHING CIRCUITIntertech Resources, Inc.1995-08-11910
K952214SIMS INTERTECH HYPERINFLATION BAG SYSTEMIntertech Resources, Inc.1995-06-08280
K952062PFT FILTERIntertech Resources, Inc.1995-06-08370
K952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRICIntertech Resources, Inc.1995-06-08310
K935036HEPA FILTERED HEAT AND MOISTURE EXCHANGERIntertech Resources, Inc.1994-01-251180
K930816HEPA FILTERED HMEIntertech Resources, Inc.1993-07-011341
K922479DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIEDIntertech Resources, Inc.1992-10-301570
K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSIntertech Resources, Inc.1992-06-30850
K912504DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIEDIntertech Resources, Inc.1991-10-231400
K912065DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIEDIntertech Resources, Inc.1991-10-231800
K911328UNIVERSAL VOLUME VENTILATOR CIRCUIT, MODIFICATIONIntertech Resources, Inc.1991-08-151420
K911298PRESSURE LIMITING ELBOW WITH MANOMETER PORTIntertech Resources, Inc.1991-06-25920
K910509PATIENT GAS SAMPLING LINE FOR OHMEDA 6000Intertech Resources, Inc.1991-04-17710
K903519INTERTECH(TM) HEAT AND MOISTURE EXCHANGERIntertech Resources, Inc.1990-12-131320
K9027331ST RESPONSE (TM) INFANT MANUAL RESUSCITATORIntertech Resources, Inc.1990-08-22620
K9005771ST RESPONSE REUSABLE MANUAL RESUSCITATOR (ADULT)Intertech Resources, Inc.1990-07-161590
K896923INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KITIntertech Resources, Inc.1990-03-12900
K894612INTERTECH NEWBORN HYPERINFLATION BAG SYSTEMIntertech Resources, Inc.1989-09-08500
K883693RESUSCITATION BAG EXHALATION FILTERIntertech Resources, Inc.1988-09-30320
K882582STERILE INHALATION WATER TRANSFER SETIntertech Resources, Inc.1988-09-301000
K882739INTERTECH LARGE VOLUME WATER TRAP (LVW)Intertech Resources, Inc.1988-08-09390
K881231DABC NONCONDUCTIVE HEATED ANESTH. BREATH. CIRCUITIntertech Resources, Inc.1988-07-011010
K881230FLEX TUBEIntertech Resources, Inc.1988-04-14230
K880304INSPIRON NEBULO BASIC EXTERNAL HEATERIntertech Resources, Inc.1988-03-04390
K871407MECONIUM ASPIRATORIntertech Resources, Inc.1987-06-15680
K870253INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATORIntertech Resources, Inc.1987-03-06430

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