PRO-FECT STERILE GAUZE SPONGES
K-Number: K962227 · 1996-08-19
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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