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)

ALGINATE/ZINC WOUND DRESSING

K-Number: K973283 · 1997-10-21

Decision Date1997-10-21
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ALGINATE/ZINC WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Technologies , Ltd.. It received FDA 510(k) clearance on 1997-10-21 under 510(k) number K973283. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ALGINATE/ZINC WOUND DRESSING?

ALGINATE/ZINC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1997-10-21. The listed applicant is Innovative Technologies , Ltd.. The 510(k) number is K973283.

When did ALGINATE/ZINC WOUND DRESSING receive FDA 510(k) clearance?

ALGINATE/ZINC WOUND DRESSING received FDA 510(k) clearance on 1997-10-21, under 510(k) number K973283.

Who is the listed applicant for ALGINATE/ZINC WOUND DRESSING?

The FDA 510(k) record lists Innovative Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALGINATE/ZINC WOUND DRESSING?

The FDA product code for ALGINATE/ZINC WOUND DRESSING is KMF.

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 Innovative Technologies , Ltd. 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 14 devices →

Related Devices (Code: KMF)

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.

↑