VISITEC NEEDLE RANGE (ORTHOPAEDIC)— 510(k) K811961

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K811961 for VISITEC NEEDLE RANGE (ORTHOPAEDIC), Substantially Equivalent on 1981-07-20. Applicant: Visitec Co..

Clearance details

Applicant: Visitec Co.
Advisory panel: Unknown
Date received: 1981-07-10
Decision date: 1981-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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