SILK SUTURES-REVISED LABELING
K-Number: K926168 · 1993-12-17
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Device Summary
Frequently Asked Questions
What is the SILK SUTURES-REVISED LABELING?
SILK SUTURES-REVISED LABELING is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Look, Inc.. The 510(k) number is K926168.
When did SILK SUTURES-REVISED LABELING receive FDA 510(k) clearance?
SILK SUTURES-REVISED LABELING received FDA 510(k) clearance on 1993-12-17, under 510(k) number K926168.
Who is the listed applicant for SILK SUTURES-REVISED LABELING?
The FDA 510(k) record lists Look, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILK SUTURES-REVISED LABELING?
The FDA product code for SILK SUTURES-REVISED LABELING is GAR.
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 Look, 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: GAR)
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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