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FDA 510(k)

LIQUAEMIN SODIUM, HEPARIN SODIUM ETC.

K-Number: K771305 · 1977-08-04

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

Device Summary

LIQUAEMIN SODIUM, HEPARIN SODIUM 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 K771305. 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 LIQUAEMIN SODIUM, HEPARIN SODIUM ETC.?

LIQUAEMIN SODIUM, HEPARIN SODIUM 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 K771305.

When did LIQUAEMIN SODIUM, HEPARIN SODIUM ETC. receive FDA 510(k) clearance?

LIQUAEMIN SODIUM, HEPARIN SODIUM ETC. received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771305.

Who is the listed applicant for LIQUAEMIN SODIUM, HEPARIN SODIUM 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 LIQUAEMIN SODIUM, HEPARIN SODIUM ETC.?

The FDA product code for LIQUAEMIN SODIUM, HEPARIN SODIUM 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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