RE-SHARPENABLE SAW BLADES
K-Number: K940501 · 1994-06-28
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Device Summary
Frequently Asked Questions
What is the RE-SHARPENABLE SAW BLADES?
RE-SHARPENABLE SAW BLADES is a medical device that received FDA 510(k) clearance on 1994-06-28. The listed applicant is Adven Medical. The 510(k) number is K940501.
When did RE-SHARPENABLE SAW BLADES receive FDA 510(k) clearance?
RE-SHARPENABLE SAW BLADES received FDA 510(k) clearance on 1994-06-28, under 510(k) number K940501.
Who is the listed applicant for RE-SHARPENABLE SAW BLADES?
The FDA 510(k) record lists Adven Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RE-SHARPENABLE SAW BLADES?
The FDA product code for RE-SHARPENABLE SAW BLADES is GFA.
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 Adven Medical 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: GFA)
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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