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FDA 510(k)

ALLIGATOR FORECPTS, CUPPED FORCEPS

K-Number: K791121 · 1979-06-27

ApplicantXomed, Inc.
Decision Date1979-06-27
Product CodeJYR
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ALLIGATOR FORECPTS, CUPPED FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K791121. The device is classified under product code JYR. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLIGATOR FORECPTS, CUPPED FORCEPS?

ALLIGATOR FORECPTS, CUPPED FORCEPS is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Xomed, Inc.. The 510(k) number is K791121.

When did ALLIGATOR FORECPTS, CUPPED FORCEPS receive FDA 510(k) clearance?

ALLIGATOR FORECPTS, CUPPED FORCEPS received FDA 510(k) clearance on 1979-06-27, under 510(k) number K791121.

Who is the listed applicant for ALLIGATOR FORECPTS, CUPPED FORCEPS?

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

What is the FDA product code for ALLIGATOR FORECPTS, CUPPED FORCEPS?

The FDA product code for ALLIGATOR FORECPTS, CUPPED FORCEPS is JYR.

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Other records listing Xomed, 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.

K002395MODEL 30 CLASSIC PNEUMATONOMETERK002987REDTRONIC XOMED MONOPOLAR ENERGIZED BLADEK002828XPS NITRO SYSTEMK002897TITANIUM MIDDLE EAR PROSTHESESK993653MICRO-FRANCE TROCARS AND ACCESSORIESK001148MEROGEL OTOLOGIC PACK

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Related Devices (Code: JYR)

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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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