STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE
K-Number: K903029 · 1990-10-25
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Device Summary
Frequently Asked Questions
What is the STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE?
STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE is a medical device that received FDA 510(k) clearance on 1990-10-25. The listed applicant is Look, Inc.. The 510(k) number is K903029.
When did STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE receive FDA 510(k) clearance?
STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE received FDA 510(k) clearance on 1990-10-25, under 510(k) number K903029.
Who is the listed applicant for STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE?
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 STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE?
The FDA product code for STERILE BLACK MONOFILAMENT NYLON NON-ABSOR. SUTURE 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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