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FDA 510(k)

PRO-FECT STERILE GAUZE SPONGES

K-Number: K962227 · 1996-08-19

Decision Date1996-08-19
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

PRO-FECT STERILE GAUZE SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Network Trading Corp. Dba Grand Intl.. It received FDA 510(k) clearance on 1996-08-19 under 510(k) number K962227. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-FECT STERILE GAUZE SPONGES?

PRO-FECT STERILE GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1996-08-19. The listed applicant is Network Trading Corp. Dba Grand Intl.. The 510(k) number is K962227.

When did PRO-FECT STERILE GAUZE SPONGES receive FDA 510(k) clearance?

PRO-FECT STERILE GAUZE SPONGES received FDA 510(k) clearance on 1996-08-19, under 510(k) number K962227.

Who is the listed applicant for PRO-FECT STERILE GAUZE SPONGES?

The FDA 510(k) record lists Network Trading Corp. Dba Grand Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-FECT STERILE GAUZE SPONGES?

The FDA product code for PRO-FECT STERILE GAUZE SPONGES 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.

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

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

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