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FDA 510(k)

FOLLICE STIMULATING HORMONE-RADIOIMM. KT

K-Number: K803279 · 1981-01-16

ApplicantImmuno Nuclear Corp.
Decision Date1981-01-16
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FOLLICE STIMULATING HORMONE-RADIOIMM. KT is the device name listed in this FDA 510(k) record. The listed applicant is Immuno Nuclear Corp.. It received FDA 510(k) clearance on 1981-01-16 under 510(k) number K803279. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOLLICE STIMULATING HORMONE-RADIOIMM. KT?

FOLLICE STIMULATING HORMONE-RADIOIMM. KT is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Immuno Nuclear Corp.. The 510(k) number is K803279.

When did FOLLICE STIMULATING HORMONE-RADIOIMM. KT receive FDA 510(k) clearance?

FOLLICE STIMULATING HORMONE-RADIOIMM. KT received FDA 510(k) clearance on 1981-01-16, under 510(k) number K803279.

Who is the listed applicant for FOLLICE STIMULATING HORMONE-RADIOIMM. KT?

The FDA 510(k) record lists Immuno Nuclear Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOLLICE STIMULATING HORMONE-RADIOIMM. KT?

The FDA product code for FOLLICE STIMULATING HORMONE-RADIOIMM. KT is CGJ.

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Other records listing Immuno Nuclear Corp. as applicant

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Related Devices (Code: CGJ)

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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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