FDA 510(k), K013289, BIOTEQUE VAGINAL PESSARIES

FDA 510(k), K013289, BIOTEQUE VAGINAL PESSARIES

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510(K) Number: K013289
Device Name: BIOTEQUE VAGINAL PESSARIES
Manufacturer:
Device Classification Name: Pessary, Vaginal
Regulation Number: 884.3575
Classification Product Code: HHW
Date Received: 10/02/2001
Decision Date: 12/27/2001
Regulation Medical Specialty: Obstetrics/Gynecology
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