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FDA 510(k)

ACTH II BY RADIOIMMUNOASSAY

K-Number: K850882 · 1985-03-21

ApplicantImmuno Nuclear Corp.
Decision Date1985-03-21
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACTH II BY RADIOIMMUNOASSAY 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 1985-03-21 under 510(k) number K850882. The device is classified under product code CKG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTH II BY RADIOIMMUNOASSAY?

ACTH II BY RADIOIMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1985-03-21. The listed applicant is Immuno Nuclear Corp.. The 510(k) number is K850882.

When did ACTH II BY RADIOIMMUNOASSAY receive FDA 510(k) clearance?

ACTH II BY RADIOIMMUNOASSAY received FDA 510(k) clearance on 1985-03-21, under 510(k) number K850882.

Who is the listed applicant for ACTH II BY RADIOIMMUNOASSAY?

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 ACTH II BY RADIOIMMUNOASSAY?

The FDA product code for ACTH II BY RADIOIMMUNOASSAY is CKG.

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Related Devices (Code: CKG)

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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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