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FDA 510(k)

STRYKER HEATED INSUFFLATOR TUBE SET

K-Number: K003792 · 2001-02-21

ApplicantStryker Corp.
Decision Date2001-02-21
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

STRYKER HEATED INSUFFLATOR TUBE SET is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2001-02-21 under 510(k) number K003792. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER HEATED INSUFFLATOR TUBE SET?

STRYKER HEATED INSUFFLATOR TUBE SET is a medical device that received FDA 510(k) clearance on 2001-02-21. The listed applicant is Stryker Corp.. The 510(k) number is K003792.

When did STRYKER HEATED INSUFFLATOR TUBE SET receive FDA 510(k) clearance?

STRYKER HEATED INSUFFLATOR TUBE SET received FDA 510(k) clearance on 2001-02-21, under 510(k) number K003792.

Who is the listed applicant for STRYKER HEATED INSUFFLATOR TUBE SET?

The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER HEATED INSUFFLATOR TUBE SET?

The FDA product code for STRYKER HEATED INSUFFLATOR TUBE SET is HIF.

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Other records listing Stryker Corp. as applicant

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K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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Related Devices (Code: HIF)

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.

K260209ENDOFLATOR+; Smart Smoke EvacuationKarl Storz SE & CO. KGK252584Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)Weyo Surgical Technology , Ltd.K252318Insufflator (OPTO-IFL1000)Guangdong Optomedic Technologies, Inc.K250388ENDOFLATOR +Karl Storz SE & CO. KGK242772AirSurgN Insufflator (10030/AirSurgN)SmartsurgN, Inc.K243527High Flow Insufflation Unit (UHI-4)Olympus Medical Systems Corporation

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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