FDA 510(k), K905069, IODOSORB GEL
FDA 510(k), K905069, IODOSORB GEL
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510(K) Number: K905069
Device Name: IODOSORB GEL
Manufacturer: PERSTORP AB C/O ROBERT JOEL SLOMOFF
Device Classification Name: Beads, Hydrophilic, For Wound Exudate Absorption
Regulation Number: 878.4018
Classification Product Code: KOZ
Date Received: 11/09/1990
Decision Date: 01/31/1991
Regulation Medical Specialty: General & Plastic Surgery
Device Name: IODOSORB GEL
Manufacturer: PERSTORP AB C/O ROBERT JOEL SLOMOFF
Device Classification Name: Beads, Hydrophilic, For Wound Exudate Absorption
Regulation Number: 878.4018
Classification Product Code: KOZ
Date Received: 11/09/1990
Decision Date: 01/31/1991
Regulation Medical Specialty: General & Plastic Surgery
- 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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