510(k) K002599
K002599 is an FDA 510(k) premarket notification submitted by Acrymed, Inc. for the device "MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045". The FDA issued a decision of Substantially Equivalent on September 21, 2000. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Acrymed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 21, 2000
- Date Received
- August 21, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound, Drug
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type