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FDA 510(k)

RE-SHARPENABLE SAW BLADES

K-Number: K940501 · 1994-06-28

ApplicantAdven Medical
Decision Date1994-06-28
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RE-SHARPENABLE SAW BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Adven Medical. It received FDA 510(k) clearance on 1994-06-28 under 510(k) number K940501. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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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