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FDA 510(k)

SENTRY INSERTION TRAY

K-Number: K942827 · 1994-11-02

ApplicantSentry Medical Products, Inc.
Decision Date1994-11-02
Product CodeFOS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SENTRY INSERTION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Sentry Medical Products, Inc.. It received FDA 510(k) clearance on 1994-11-02 under 510(k) number K942827. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENTRY INSERTION TRAY?

SENTRY INSERTION TRAY is a medical device that received FDA 510(k) clearance on 1994-11-02. The listed applicant is Sentry Medical Products, Inc.. The 510(k) number is K942827.

When did SENTRY INSERTION TRAY receive FDA 510(k) clearance?

SENTRY INSERTION TRAY received FDA 510(k) clearance on 1994-11-02, under 510(k) number K942827.

Who is the listed applicant for SENTRY INSERTION TRAY?

The FDA 510(k) record lists Sentry Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENTRY INSERTION TRAY?

The FDA product code for SENTRY INSERTION TRAY is FOS.

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Other records listing Sentry Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962122SENTRY RADIOTRANSLUCENT ECG ELECTRODESK955636SENTRY DISPOSABLE DISPERSIVE ELECTRODEK934000SENTRY AQUEOUS GEL ECG ELECTRODESK935098BABY BOARDK933603LEADWIREK932704PATIENT CABLE

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Related Devices (Code: FOS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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