CONVERSE-GILLIES NEEDLE HOLDER— 510(k) K772388

Name: FDA 510(k) clearance K772388
Creator: U.S. Food and Drug Administration
Published: 1978-01-20

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K772388 for CONVERSE-GILLIES NEEDLE HOLDER, Substantially Equivalent on 1978-01-20. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HXK
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1977-12-27
Decision date: 1978-01-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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