Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CYCLIC ADENOSINE MONOPHOSHATE BY RADIO

K-Number: K823504 · 1983-01-28

Decision Date1983-01-28
Product CodeCHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CYCLIC ADENOSINE MONOPHOSHATE BY RADIO 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 1983-01-28 under 510(k) number K823504. The device is classified under product code CHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYCLIC ADENOSINE MONOPHOSHATE BY RADIO?

CYCLIC ADENOSINE MONOPHOSHATE BY RADIO is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Immuno Nuclear Corp.. The 510(k) number is K823504.

When did CYCLIC ADENOSINE MONOPHOSHATE BY RADIO receive FDA 510(k) clearance?

CYCLIC ADENOSINE MONOPHOSHATE BY RADIO received FDA 510(k) clearance on 1983-01-28, under 510(k) number K823504.

Who is the listed applicant for CYCLIC ADENOSINE MONOPHOSHATE BY RADIO?

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 CYCLIC ADENOSINE MONOPHOSHATE BY RADIO?

The FDA product code for CYCLIC ADENOSINE MONOPHOSHATE BY RADIO is CHO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Immuno Nuclear Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 30 devices →

Related Devices (Code: CHO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑