N80-838 SUPRAMID EXTRA SUTURE
K-Number: K912429 · 1991-10-02
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Device Summary
Frequently Asked Questions
What is the N80-838 SUPRAMID EXTRA SUTURE?
N80-838 SUPRAMID EXTRA SUTURE is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is S. Jackson, Inc.. The 510(k) number is K912429.
When did N80-838 SUPRAMID EXTRA SUTURE receive FDA 510(k) clearance?
N80-838 SUPRAMID EXTRA SUTURE received FDA 510(k) clearance on 1991-10-02, under 510(k) number K912429.
Who is the listed applicant for N80-838 SUPRAMID EXTRA SUTURE?
The FDA 510(k) record lists S. Jackson, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for N80-838 SUPRAMID EXTRA SUTURE?
The FDA product code for N80-838 SUPRAMID EXTRA 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 S. Jackson, 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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