BIOSELF 2000 FERTILITY INDICATOR— 510(k) K904211

Name: FDA 510(k) clearance K904211
Creator: U.S. Food and Drug Administration
Published: 1992-10-14

Substantially Equivalent

Bioself, Inc.

FDA 510(k) clearance K904211 for BIOSELF 2000 FERTILITY INDICATOR, Substantially Equivalent on 1992-10-14. Applicant: Bioself, Inc.. Device class: Unclassified.

Clearance details

Applicant: Bioself, Inc.
Product code: Code LHD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1990-09-12
Decision date: 1992-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thonex-Geneve-Suisse, CH

Download summary PDF View on FDA.gov ↗

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