25-450 TO 25-540 VARIOUS SUTURE FORCEPS
K-Number: K851782 · 1985-06-20
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Device Summary
Frequently Asked Questions
What is the 25-450 TO 25-540 VARIOUS SUTURE FORCEPS?
25-450 TO 25-540 VARIOUS SUTURE FORCEPS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851782.
When did 25-450 TO 25-540 VARIOUS SUTURE FORCEPS receive FDA 510(k) clearance?
25-450 TO 25-540 VARIOUS SUTURE FORCEPS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851782.
Who is the listed applicant for 25-450 TO 25-540 VARIOUS SUTURE FORCEPS?
The FDA 510(k) record lists Artiberia as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 25-450 TO 25-540 VARIOUS SUTURE FORCEPS?
The FDA product code for 25-450 TO 25-540 VARIOUS SUTURE FORCEPS is GDL.
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 Artiberia 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: GDL)
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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