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FDA 510(k)

HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL

K-Number: K920826 · 1992-04-07

ApplicantEastman Kodak Company
Decision Date1992-04-07
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1992-04-07 under 510(k) number K920826. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL?

HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL is a medical device that received FDA 510(k) clearance on 1992-04-07. The listed applicant is Eastman Kodak Company. The 510(k) number is K920826.

When did HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL receive FDA 510(k) clearance?

HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL received FDA 510(k) clearance on 1992-04-07, under 510(k) number K920826.

Who is the listed applicant for HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL?

The FDA product code for HUMAN CHORIONIC GONADATROPHIN AND UNCON. ESTRIOL is JJY.

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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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