GAUZE SPONGES
K-Number: K924650 · 1993-01-11
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Device Summary
Frequently Asked Questions
What is the GAUZE SPONGES?
GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1993-01-11. The listed applicant is Dav-Mar Medical Products, Inc.. The 510(k) number is K924650.
When did GAUZE SPONGES receive FDA 510(k) clearance?
GAUZE SPONGES received FDA 510(k) clearance on 1993-01-11, under 510(k) number K924650.
Who is the listed applicant for GAUZE SPONGES?
The FDA 510(k) record lists Dav-Mar Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE SPONGES?
The FDA product code for GAUZE SPONGES is NAB.
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 Dav-Mar Medical Products, 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: NAB)
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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