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FDA 510(k), K013086, WET LIGHT PERSONAL MOISTURIZER
FDA 510(k), K013086, WET LIGHT PERSONAL MOISTURIZER
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510(K) Number: K013086
Device Name: WET LIGHT PERSONAL MOISTURIZER
Manufacturer: TRIGG LABORATORIES, INC.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 09/14/2001
Decision Date: 12/13/2001
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: WET LIGHT PERSONAL MOISTURIZER
Manufacturer: TRIGG LABORATORIES, INC.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 09/14/2001
Decision Date: 12/13/2001
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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