13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS
K-Number: K851756 · 1985-06-20
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Device Summary
Frequently Asked Questions
What is the 13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS?
13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851756.
When did 13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS receive FDA 510(k) clearance?
13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851756.
Who is the listed applicant for 13-180 TO 13-212 VARIOUS MODELS OF MAYO SCISSORS?
The FDA 510(k) record lists Artiberia as the applicant. This does not by itself establish the device manufacturer.
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.
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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