MICROGYN PLUS STIMULATION DEVICE— 510(k) K963222

Substantially Equivalent

Hollister, Inc.

FDA 510(k) clearance K963222 for MICROGYN PLUS STIMULATION DEVICE, Substantially Equivalent on 1996-10-23. Applicant: Hollister, Inc..

Clearance details

Applicant: Hollister, Inc.
Product code: Code KPI
Advisory panel: Gastroenterology, Urology
Date received: 1996-08-16
Decision date: 1996-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Libertyville, IL, US

Download summary PDF View on FDA.gov ↗

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