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)

DUKAL NON-WOVEN GAUZE

K-Number: K940440 · 1994-03-09

ApplicantDukal Corp.
Decision Date1994-03-09
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

DUKAL NON-WOVEN GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Dukal Corp.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K940440. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUKAL NON-WOVEN GAUZE?

DUKAL NON-WOVEN GAUZE is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is Dukal Corp.. The 510(k) number is K940440.

When did DUKAL NON-WOVEN GAUZE receive FDA 510(k) clearance?

DUKAL NON-WOVEN GAUZE received FDA 510(k) clearance on 1994-03-09, under 510(k) number K940440.

Who is the listed applicant for DUKAL NON-WOVEN GAUZE?

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

What is the FDA product code for DUKAL NON-WOVEN GAUZE?

The FDA product code for DUKAL NON-WOVEN GAUZE is EFQ.

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 Dukal 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 11 devices →

Related Devices (Code: EFQ)

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.

↑