RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET— 510(k) K884696

Substantially Equivalent

Laboratoire Ccd C/O Washington Regulatory Services

FDA 510(k) clearance K884696 for RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET, Substantially Equivalent on 1989-01-27. Applicant: Laboratoire Ccd C/O Washington Regulatory Services.

Clearance details

Applicant: Laboratoire Ccd C/O Washington Regulatory Services
Product code: Code HDR
Advisory panel: Obstetrics/Gynecology
Date received: 1988-11-09
Decision date: 1989-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ringoes, NJ, US

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