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Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Marquest Medical Products, Inc. · Predicate Candidate Screening

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

69 daysmedian FDA review time
175 days90th percentile
32clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K050066C-CO2 COLORIMETRIC CO2 INDICATORMarquest Medical Products, Inc.2005-03-01480
K970478SCT 3000 HEATED HUMIDIFIERMarquest Medical Products, Inc.1997-07-161590
K962220HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIERMarquest Medical Products, Inc.1997-01-142180
K962223WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIERMarquest Medical Products, Inc.1997-01-142180
K960972DISPOSABLE GAS SAMPLING INTERFACE KITSMarquest Medical Products, Inc.1996-10-182210
K961838RESPIRGARD II, SPIROGARDMarquest Medical Products, Inc.1996-10-181580
K904690TEMP MARQ(TM) CONVECTIVE WARMING SYSTEMMarquest Medical Products, Inc.1991-02-011080
K903138MARQUEST SCT 3000, HEATED HUMIDIFICATION SYSTEMMarquest Medical Products, Inc.1990-10-11860
K902632GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERSMarquest Medical Products, Inc.1990-09-04820
K903307TEMP MARQ TEMPERATURE TREND INDICATORMarquest Medical Products, Inc.1990-08-17240
K880979MARQUEST SCT 2000, HEATED HUMIDIFICATION SYSTEMMarquest Medical Products, Inc.1988-07-151290
K874395RESPIRGARD II NEBULIZER SYSTEMMarquest Medical Products, Inc.1987-12-21540
K863918MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT.Marquest Medical Products, Inc.1987-01-07910
K855024MARQUEST QC-IV TONOMETERMarquest Medical Products, Inc.1986-04-071110
K853056RESPIR GARD-II FACE MASK CORRUGATED TUBINGMarquest Medical Products, Inc.1985-08-07190
K842008MARQUEST MICRO STIK 9000 SERIESMarquest Medical Products, Inc.1984-05-2580
K840966ANESTHETIC GAS MONITOR SYSMarquest Medical Products, Inc.1984-05-14690
K833973MINOLTA SM-32 OXYGEN SATURATION MONITMarquest Medical Products, Inc.1984-05-091750
K840740CIRCUIT BREATHINGMarquest Medical Products, Inc.1984-04-17600
K840535DISPOS. ANESTHESIA FACE MASKMarquest Medical Products, Inc.1984-02-21130
K833269RESPIR GARD BACTERIA FILTERMarquest Medical Products, Inc.1983-10-31400
K833267RESPIR GARD-II OXYGARD HYDROGARD-SPIROMarquest Medical Products, Inc.1983-10-28370
K830310OMNISTICKMarquest Medical Products, Inc.1983-05-251190
K830311AUTO STIKMarquest Medical Products, Inc.1983-05-251190
K830312ASPIRATORMarquest Medical Products, Inc.1983-05-251190
K823714DISPOSABLE NON-REBREATHING ANES. CIRCUITMarquest Medical Products, Inc.1983-01-07280
K822379DISPOSABLE ANESTHESIA BREATHING CIRCUITMarquest Medical Products, Inc.1982-08-20110
K820875AUTOSTIKMarquest Medical Products, Inc.1982-05-07390
K811700CIRCUIT, BREATHINGMarquest Medical Products, Inc.1981-07-10240
K802763RESPIRGARDMarquest Medical Products, Inc.1980-11-26220
K801620ASPIRATORMarquest Medical Products, Inc.1980-07-2160
K800860OMNISTIK, MQ 501GSMarquest Medical Products, Inc.1980-04-29130

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