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)

HUMAN INTRACT PARATHYROID HORMONE BY

K-Number: K830664 · 1983-05-09

Decision Date1983-05-09
Product CodeCEW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HUMAN INTRACT PARATHYROID HORMONE BY 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 1983-05-09 under 510(k) number K830664. The device is classified under product code CEW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN INTRACT PARATHYROID HORMONE BY?

HUMAN INTRACT PARATHYROID HORMONE BY is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Immuno Nuclear Corp.. The 510(k) number is K830664.

When did HUMAN INTRACT PARATHYROID HORMONE BY receive FDA 510(k) clearance?

HUMAN INTRACT PARATHYROID HORMONE BY received FDA 510(k) clearance on 1983-05-09, under 510(k) number K830664.

Who is the listed applicant for HUMAN INTRACT PARATHYROID HORMONE BY?

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 HUMAN INTRACT PARATHYROID HORMONE BY?

The FDA product code for HUMAN INTRACT PARATHYROID HORMONE BY is CEW.

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: CEW)

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.

↑