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FDA 510(k)

SHEATH, RESECTOSCOPE

K-Number: K760182 · 1976-12-02

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-12-02
Product CodeFDC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SHEATH, RESECTOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K760182. The device is classified under product code FDC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEATH, RESECTOSCOPE?

SHEATH, RESECTOSCOPE is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760182.

When did SHEATH, RESECTOSCOPE receive FDA 510(k) clearance?

SHEATH, RESECTOSCOPE received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760182.

Who is the listed applicant for SHEATH, RESECTOSCOPE?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHEATH, RESECTOSCOPE?

The FDA product code for SHEATH, RESECTOSCOPE is FDC.

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Other records listing V. Mueller O.V. Baxter Healthcare Corp. as applicant

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Related Devices (Code: FDC)

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.

K021166ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BRAcmi-Circon CorporationK992141OLYMPUS WORKING ELEMENT FOR PROBESOlympus Winter & Ibe GmbHK991426MAHE INSTRUMENTSMahe Intl., Inc.K942626CONTINUOUS FLOW BIOPSY PROBEGm Engineering, Inc.K933962GM CONTINUOUS FLOW BIOPSY PROBEGm Engineering, Inc.K895643MODIFIED UROPUMP* FLUID MANAGEMENT SYSTEMOrthoconcept, 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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