GAUZE COMPRESS
K-Number: K960615 · 1996-11-25
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Device Summary
Frequently Asked Questions
What is the GAUZE COMPRESS?
GAUZE COMPRESS is a medical device that received FDA 510(k) clearance on 1996-11-25. The listed applicant is Certified Safety Mfg., Inc.. The 510(k) number is K960615.
When did GAUZE COMPRESS receive FDA 510(k) clearance?
GAUZE COMPRESS received FDA 510(k) clearance on 1996-11-25, under 510(k) number K960615.
Who is the listed applicant for GAUZE COMPRESS?
The FDA 510(k) record lists Certified Safety Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE COMPRESS?
The FDA product code for GAUZE COMPRESS 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 Certified Safety Mfg., Inc. 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: 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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