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FDA 510(k)

LABELED HUMAN CHORIONIC GONADOTROPHIN

K-Number: K790876 · 1979-07-17

ApplicantPcl-Ria, Inc.
Decision Date1979-07-17
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LABELED HUMAN CHORIONIC GONADOTROPHIN is the device name listed in this FDA 510(k) record. The listed applicant is Pcl-Ria, Inc.. It received FDA 510(k) clearance on 1979-07-17 under 510(k) number K790876. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABELED HUMAN CHORIONIC GONADOTROPHIN?

LABELED HUMAN CHORIONIC GONADOTROPHIN is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Pcl-Ria, Inc.. The 510(k) number is K790876.

When did LABELED HUMAN CHORIONIC GONADOTROPHIN receive FDA 510(k) clearance?

LABELED HUMAN CHORIONIC GONADOTROPHIN received FDA 510(k) clearance on 1979-07-17, under 510(k) number K790876.

Who is the listed applicant for LABELED HUMAN CHORIONIC GONADOTROPHIN?

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

What is the FDA product code for LABELED HUMAN CHORIONIC GONADOTROPHIN?

The FDA product code for LABELED HUMAN CHORIONIC GONADOTROPHIN is JHI.

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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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