510(k) K911682
K911682 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "AIRSTRIP FIRST AID & POST-OP DRESSING". The FDA issued a decision of Substantially Equivalent on July 17, 1991. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 17, 1991
- Date Received
- April 15, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tape And Bandage, Adhesive
- Device Class
- Class I
- Regulation Number
- 880.5240
- Review Panel
- SU
- Submission Type