FDA 510(k)

CONVERSE ALTAR RETRACTOR

K-Number: K760851 · 1977-03-10

ApplicantV. Mueller O.V. Baxter Healthcare Corp.

Decision Date1977-03-10

Product CodeKAL

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

CONVERSE ALTAR RETRACTOR 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 1977-03-10 under 510(k) number K760851. The device is classified under product code KAL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERSE ALTAR RETRACTOR?

CONVERSE ALTAR RETRACTOR is a medical device that received FDA 510(k) clearance on 1977-03-10. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760851.

When did CONVERSE ALTAR RETRACTOR receive FDA 510(k) clearance?

CONVERSE ALTAR RETRACTOR received FDA 510(k) clearance on 1977-03-10, under 510(k) number K760851.

Who is the listed applicant for CONVERSE ALTAR RETRACTOR?

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 CONVERSE ALTAR RETRACTOR?

The FDA product code for CONVERSE ALTAR RETRACTOR is KAL.

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

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Related Devices (Code: KAL)

K870758SMALL MASTOID RETRACTORTreace Medical, Inc.K833604ADJUSTABLE FORK RETRACTORMicrotek Medical, Inc.K772381RING HANDLE & RETRACTORSEdward Weck, Inc.K772392ALLPORT MASTOID RETRACTORSEdward Weck, 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.