MICROGYN PLUS STIMULATION DEVICE— 510(k) K013141

Substantially Equivalent

Hollister, Inc.

FDA 510(k) clearance K013141 for MICROGYN PLUS STIMULATION DEVICE, Substantially Equivalent on 2001-12-19. Applicant: Hollister, Inc..

Clearance details

Applicant: Hollister, Inc.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 2001-09-20
Decision date: 2001-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Libertyville, IL, US

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