CERVICAL SPATULA— 510(k) K811548

Substantially Equivalent

Procedure Products, Inc.

FDA 510(k) clearance K811548 for CERVICAL SPATULA, Substantially Equivalent on 1981-06-23. Applicant: Procedure Products, Inc..

Clearance details

Applicant: Procedure Products, Inc.
Product code: Code HHT
Advisory panel: Obstetrics/Gynecology
Date received: 1981-06-01
Decision date: 1981-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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