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)

CLASS OF CASTING ALLOYS TYPE III OR ALT

K-Number: K820434 · 1982-03-11

Decision Date1982-03-11
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLASS OF CASTING ALLOYS TYPE III OR ALT is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1982-03-11 under 510(k) number K820434. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLASS OF CASTING ALLOYS TYPE III OR ALT?

CLASS OF CASTING ALLOYS TYPE III OR ALT is a medical device that received FDA 510(k) clearance on 1982-03-11. The listed applicant is Howmedica Corp.. The 510(k) number is K820434.

When did CLASS OF CASTING ALLOYS TYPE III OR ALT receive FDA 510(k) clearance?

CLASS OF CASTING ALLOYS TYPE III OR ALT received FDA 510(k) clearance on 1982-03-11, under 510(k) number K820434.

Who is the listed applicant for CLASS OF CASTING ALLOYS TYPE III OR ALT?

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

What is the FDA product code for CLASS OF CASTING ALLOYS TYPE III OR ALT?

The FDA product code for CLASS OF CASTING ALLOYS TYPE III OR ALT is EJS.

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 Howmedica 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 373 devices →

Related Devices (Code: EJS)

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.

↑