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)

STERILE COTTON ROLLS #3, 1 1/2

K-Number: K830175 · 1983-02-18

ApplicantVeratex Corp.
Decision Date1983-02-18
Product CodeEFN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERILE COTTON ROLLS #3, 1 1/2 is the device name listed in this FDA 510(k) record. The listed applicant is Veratex Corp.. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K830175. The device is classified under product code EFN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE COTTON ROLLS #3, 1 1/2?

STERILE COTTON ROLLS #3, 1 1/2 is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Veratex Corp.. The 510(k) number is K830175.

When did STERILE COTTON ROLLS #3, 1 1/2 receive FDA 510(k) clearance?

STERILE COTTON ROLLS #3, 1 1/2 received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830175.

Who is the listed applicant for STERILE COTTON ROLLS #3, 1 1/2?

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

What is the FDA product code for STERILE COTTON ROLLS #3, 1 1/2?

The FDA product code for STERILE COTTON ROLLS #3, 1 1/2 is EFN.

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 Veratex 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.

Related Devices (Code: EFN)

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.

↑