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.. Device class: 2.

Clearance details

Applicant: Telesis Corp.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1980-07-29
Decision date: 1980-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FLK

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K960224 — GERATHERM MERCUIRY FREE CLINICAL THERMOMETER1996-03-25
K953465 — KENTEMP1995-12-15
K942483 — CLINICAL GLASS THERMOMETER1995-03-28
K941673 — MEDIAID UNIVERSAL THERMOMETER1994-08-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.