OVULON MONITOR— 510(k) K973860

Substantially Equivalent

Conception Technology, Inc.

FDA 510(k) clearance K973860 for OVULON MONITOR, Substantially Equivalent on 1998-01-07. Applicant: Conception Technology, Inc.. Device class: 1.

Clearance details

Applicant: Conception Technology, Inc.
Product code: Code NGE
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1997-10-09
Decision date: 1998-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft. Collins, CO, US

Download summary PDF View on FDA.gov ↗

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K850579 — CUE FERTILITY MONITOR1985-03-22

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