510(k) K801884
K801884 is an FDA 510(k) premarket notification submitted by Acme United Corp. for the device "OP-SITE SKIN CLOSURE SUTURE ADHESIVE". The FDA issued a decision of Substantially Equivalent on October 10, 1980. The device falls under product code FPX (Strip, Adhesive, Closure, Skin), a Class I device regulated under 21 CFR 880.5240. Acme United Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 10, 1980
- Date Received
- August 7, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Strip, Adhesive, Closure, Skin
- Device Class
- Class I
- Regulation Number
- 880.5240
- Review Panel
- SU
- Submission Type