510(k) K983184
K983184 is an FDA 510(k) premarket notification submitted by Molnlycke Health Care, Inc. for the device "MEPILEX". The FDA issued a decision of Substantially Equivalent on October 28, 1998. The device falls under product code MGP (Dressing, Wound And Burn, Occlusive), a Class U device. Molnlycke Health Care, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1998
- Date Received
- September 11, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound And Burn, Occlusive
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type