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FDA 510(k)

HUMAN CHORIONIC GONADOTROPHIN STANDARDS

K-Number: K790863 · 1979-07-17

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

Device Summary

HUMAN CHORIONIC GONADOTROPHIN STANDARDS 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 K790863. 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 HUMAN CHORIONIC GONADOTROPHIN STANDARDS?

HUMAN CHORIONIC GONADOTROPHIN STANDARDS 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 K790863.

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

HUMAN CHORIONIC GONADOTROPHIN STANDARDS received FDA 510(k) clearance on 1979-07-17, under 510(k) number K790863.

Who is the listed applicant for HUMAN CHORIONIC GONADOTROPHIN STANDARDS?

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 HUMAN CHORIONIC GONADOTROPHIN STANDARDS?

The FDA product code for HUMAN CHORIONIC GONADOTROPHIN STANDARDS 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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