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)

NON-ABSORBENT TOWELS

K-Number: K813519 · 1982-01-05

Decision Date1982-01-05
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-ABSORBENT TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Cunningham Woodland, Inc.. It received FDA 510(k) clearance on 1982-01-05 under 510(k) number K813519. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-ABSORBENT TOWELS?

NON-ABSORBENT TOWELS is a medical device that received FDA 510(k) clearance on 1982-01-05. The listed applicant is Cunningham Woodland, Inc.. The 510(k) number is K813519.

When did NON-ABSORBENT TOWELS receive FDA 510(k) clearance?

NON-ABSORBENT TOWELS received FDA 510(k) clearance on 1982-01-05, under 510(k) number K813519.

Who is the listed applicant for NON-ABSORBENT TOWELS?

The FDA 510(k) record lists Cunningham Woodland, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NON-ABSORBENT TOWELS?

The FDA product code for NON-ABSORBENT TOWELS is KME.

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 Cunningham Woodland, Inc. 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 10 devices →

Related Devices (Code: KME)

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.

↑