BAYONET SURGICAL INSTRUMENTS— 510(k) K772371

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K772371 for BAYONET SURGICAL INSTRUMENTS, Substantially Equivalent on 1978-01-06. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1977-12-27
Decision date: 1978-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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