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FDA 510(k)

ZIMMER SURGICAL INSTRUMENT LUBRICANT

K-Number: K790331 · 1979-04-03

ApplicantZimmer, Inc.
Decision Date1979-04-03
Product Code
DecisionSubstantially Equivalent

Device Summary

ZIMMER SURGICAL INSTRUMENT LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1979-04-03 under 510(k) number K790331. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER SURGICAL INSTRUMENT LUBRICANT?

ZIMMER SURGICAL INSTRUMENT LUBRICANT is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Zimmer, Inc.. The 510(k) number is K790331.

When did ZIMMER SURGICAL INSTRUMENT LUBRICANT receive FDA 510(k) clearance?

ZIMMER SURGICAL INSTRUMENT LUBRICANT received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790331.

Who is the listed applicant for ZIMMER SURGICAL INSTRUMENT LUBRICANT?

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

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Other records listing Zimmer, Inc. as applicant

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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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