9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS
K-Number: K851752 · 1985-06-20
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Device Summary
Frequently Asked Questions
What is the 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS?
9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851752.
When did 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS receive FDA 510(k) clearance?
9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851752.
Who is the listed applicant for 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS?
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 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS?
The FDA product code for 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS is GDN.
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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