FDA 510(k)

SURGICAL GAUZE

K-Number: K823455 · 1983-01-28

Decision Date1983-01-28

Product Code

DecisionSubstantially Equivalent

Device Summary

SURGICAL GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Worldwide Surgical Gauze. It received FDA 510(k) clearance on 1983-01-28 under 510(k) number K823455. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL GAUZE?

SURGICAL GAUZE is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Worldwide Surgical Gauze. The 510(k) number is K823455.

When did SURGICAL GAUZE receive FDA 510(k) clearance?

SURGICAL GAUZE received FDA 510(k) clearance on 1983-01-28, under 510(k) number K823455.

Who is the listed applicant for SURGICAL GAUZE?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Worldwide Surgical Gauze as applicant

K812572GAUZE SPONGES K803172GAUZE SPONGES K802429COTTON ROLLS

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.