FERTILITY AWARENESS METHOD KIT— 510(k) K801791

Substantially Equivalent

Telesis Corp.

FDA 510(k) clearance K801791 for FERTILITY AWARENESS METHOD KIT, Substantially Equivalent on 1980-10-31. Applicant: Telesis Corp..

Clearance details

Applicant: Telesis Corp.
Product code: Code FLK
Advisory panel: General Hospital
Date received: 1980-07-29
Decision date: 1980-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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