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FDA 510(k)

LIQUAEMIB SODIUM PRESERVATIVE, ETC.

K-Number: K771304 · 1977-08-04

ApplicantOrganon, Inc.
Decision Date1977-08-04
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUAEMIB SODIUM PRESERVATIVE, ETC. is the device name listed in this FDA 510(k) record. The listed applicant is Organon, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771304. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUAEMIB SODIUM PRESERVATIVE, ETC.?

LIQUAEMIB SODIUM PRESERVATIVE, ETC. is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Organon, Inc.. The 510(k) number is K771304.

When did LIQUAEMIB SODIUM PRESERVATIVE, ETC. receive FDA 510(k) clearance?

LIQUAEMIB SODIUM PRESERVATIVE, ETC. received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771304.

Who is the listed applicant for LIQUAEMIB SODIUM PRESERVATIVE, ETC.?

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

What is the FDA product code for LIQUAEMIB SODIUM PRESERVATIVE, ETC.?

The FDA product code for LIQUAEMIB SODIUM PRESERVATIVE, ETC. is GIM.

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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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