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)

RIANEN CYCLIC-AMP RADIOIMMUNOASSAY

K-Number: K841478 · 1984-06-14

Decision Date1984-06-14
Product CodeCHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIANEN CYCLIC-AMP RADIOIMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is New England Nuclear. It received FDA 510(k) clearance on 1984-06-14 under 510(k) number K841478. 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 RIANEN CYCLIC-AMP RADIOIMMUNOASSAY?

RIANEN CYCLIC-AMP RADIOIMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1984-06-14. The listed applicant is New England Nuclear. The 510(k) number is K841478.

When did RIANEN CYCLIC-AMP RADIOIMMUNOASSAY receive FDA 510(k) clearance?

RIANEN CYCLIC-AMP RADIOIMMUNOASSAY received FDA 510(k) clearance on 1984-06-14, under 510(k) number K841478.

Who is the listed applicant for RIANEN CYCLIC-AMP RADIOIMMUNOASSAY?

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

What is the FDA product code for RIANEN CYCLIC-AMP RADIOIMMUNOASSAY?

The FDA product code for RIANEN CYCLIC-AMP RADIOIMMUNOASSAY 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 New England Nuclear 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 18 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.

↑