GAUZE CHERRY SPONGE
K-Number: K872809 · 1987-08-04
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Device Summary
Frequently Asked Questions
What is the GAUZE CHERRY SPONGE?
GAUZE CHERRY SPONGE is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is American Silk Sutures, Inc.. The 510(k) number is K872809.
When did GAUZE CHERRY SPONGE receive FDA 510(k) clearance?
GAUZE CHERRY SPONGE received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872809.
Who is the listed applicant for GAUZE CHERRY SPONGE?
The FDA 510(k) record lists American Silk Sutures, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE CHERRY SPONGE?
The FDA product code for GAUZE CHERRY SPONGE is GDY.
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 American Silk Sutures, 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: GDY)
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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