KNIFE MAKER— 510(k) K863616

Substantially Equivalent

Surgipath Medical Industries, Inc.

FDA 510(k) clearance K863616 for KNIFE MAKER, Substantially Equivalent on 1986-09-25. Applicant: Surgipath Medical Industries, Inc..

Clearance details

Applicant: Surgipath Medical Industries, Inc.
Product code: Code IDL
Advisory panel: Pathology
Date received: 1986-09-16
Decision date: 1986-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grayslake, IL, US

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