GAUZE PADS STERILE SINGLES
K-Number: K802862 · 1980-12-11
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Device Summary
Frequently Asked Questions
What is the GAUZE PADS STERILE SINGLES?
GAUZE PADS STERILE SINGLES is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K802862.
When did GAUZE PADS STERILE SINGLES receive FDA 510(k) clearance?
GAUZE PADS STERILE SINGLES received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802862.
Who is the listed applicant for GAUZE PADS STERILE SINGLES?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE PADS STERILE SINGLES?
The FDA product code for GAUZE PADS STERILE SINGLES 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 Abco Dealers, 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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