510(k) K801884

OP-SITE SKIN CLOSURE SUTURE ADHESIVE by Acme United Corp. — Product Code FPX

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