Atlas FDA

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

BSK — Predicate Candidate Screening

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

146 daysmedian FDA review time
363 days90th percentile
39clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K243562CuffGuardIdmed2025-08-122670
K242642CuffTrekShanghai Longmann Tech Co., Ltd.2025-03-071850
K220854TrachCuff Cuff ControllerAw Technologies Aps2023-04-143870
K221477AG100sHospitech Respiration , Ltd.2022-12-292200
K202874Puritan Bennett Cuff Pressure ManagerCovidien, LLC2021-01-091031
K192611CuffixBiovo Technologies , Ltd.2020-08-133280
K191858Pylant MonitorKal-Med, LLC2020-02-242280
K182548Accucuff Cuff Pressure IndicatorTianjin Medis Medical Device Co., Ltd.2019-01-251300
K180991AG 100sHospitech Respiration , Ltd.2018-10-121790
K173914VORTRAN Cuff Inflator (VCI)Vortran Medical Technology 1, Inc.2018-05-251540
K152778TRACOE Cuff Pressure MonitorTracoe Medical GmbH2016-12-214530
K152865TRACOE smart Cuff ManagerTracoe Medical GmbH2016-09-273630
K150157AnapnoGuard 100 Respiratory Guard SystemHospitech Respiration , Ltd.2016-02-163890
K150893IntelliCuffHamilton Medical AG2016-01-293021
K142103CUFF PILOT, SURE SEALTeleflexmedical, Inc.2015-05-082800
K122721AG GUFFILLHospitech Respiration , Ltd.2013-05-032400
K112915SPIRTIUS CUFF INFLATION SYRINGESpiritus Technologies, LLC2012-05-252350
K113644PILOT TUBE REPAIR KITInstrumentation Industries, Inc.2012-01-26450
K110631VENNER TRACHEAL SEAL MONITORVenner Medical (Singapore) Pte, Ltd.2011-07-281460
K102674CUFF SENTRYVentlab Corp.2011-07-223090
K102704EASY CUFFJoan Spiegel, MD2011-03-101710
K092733PYTONArm Medical Devices, Inc.2010-02-261750
K081805CUFFALERTSunmed2008-11-141410
K973755PILOT TUBE REPAIR KITInstrumentation Industries, Inc.1997-12-17760
K951046RUSCH ENDOTEST CUFF PRESSURE MONITORRusch Intl.1995-04-06310
K923800PRESSURE GAUGEInnovations For Mechanical Ventilation, Inc.1993-02-262120
K912352PEACE MODEL 100 CUFF MONITORPeace Medical, Inc.1991-08-02660
K912723POSEY CUFFLATORPosey Co.1991-07-20310
K902114CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITORDiemolding Corp.1990-07-18680
K900755DIGITAL CUFF PV GAUGEInternational Medical Products, Inc.1990-04-26690
K901255CUFF BARO GUARD OR CBG ABBREVIATEDNelson Engineering, Inc.1990-03-28130
K885216ATTACHABLE LANZ (TENTATIVE)Mallinckroot, Inc.1989-03-14850
K884638BE 410 ENDOTRACHEAL TUBE/TRACH TUBE, PILOT REPAIRInstrumentation Industries, Inc.1988-11-23160
K881514PRISTINE SPECIMEN TUBE AND INTRODUCER SYSTEMHall Laboratories, Inc.1988-06-16660
K881178CUFFCHECKDhd Medical Products Div. Diemolding Corp.1988-04-14270
K873614CBG CUFF MANOMETERBio-Med Devices, Inc.1988-01-221360
K833327RESPIRONICS PR VALVERespironics, Inc.1983-11-28620
K831577TRACHEA/CUFF INFLATOR W/PRESSURE #583Medical Electronics Corp.1983-07-07510
K792265SHILEY PRESSURE RELIEF ADAPTER PRAShiley, Inc.1979-11-27180

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