GENDER CHOICE INFORMATION KIT, FEMALE AND MALE— 510(k) K870999

Name: FDA 510(k) clearance K870999
Creator: U.S. Food and Drug Administration
Published: 1987-07-14

Substantially Equivalent

Procare C/O Wiley, Rein & Fielding

FDA 510(k) clearance K870999 for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE, Substantially Equivalent on 1987-07-14. Applicant: Procare C/O Wiley, Rein & Fielding. Device class: Unclassified.

Clearance details

Applicant: Procare C/O Wiley, Rein & Fielding
Product code: Product code LHD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1987-03-11
Decision date: 1987-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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