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)

ALLDRESS MULTI LAYERED WOUND DRESSING

K-Number: K945206 · 1995-01-12

Decision Date1995-01-12
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALLDRESS MULTI LAYERED WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Scott Health Care. It received FDA 510(k) clearance on 1995-01-12 under 510(k) number K945206. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLDRESS MULTI LAYERED WOUND DRESSING?

ALLDRESS MULTI LAYERED WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-01-12. The listed applicant is Scott Health Care. The 510(k) number is K945206.

When did ALLDRESS MULTI LAYERED WOUND DRESSING receive FDA 510(k) clearance?

ALLDRESS MULTI LAYERED WOUND DRESSING received FDA 510(k) clearance on 1995-01-12, under 510(k) number K945206.

Who is the listed applicant for ALLDRESS MULTI LAYERED WOUND DRESSING?

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

What is the FDA product code for ALLDRESS MULTI LAYERED WOUND DRESSING?

The FDA product code for ALLDRESS MULTI LAYERED 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 Scott Health Care 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 9 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.

↑