510(k) K802785

ELASTIC BANDAGE by Secol Co. — Product Code FQM

K802785 is an FDA 510(k) premarket notification submitted by Secol Co. for the device "ELASTIC BANDAGE". The FDA issued a decision of Substantially Equivalent on December 11, 1980. The device falls under product code FQM (Bandage, Elastic), a Class I device regulated under 21 CFR 880.5075. Secol Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 11, 1980
Date Received
November 4, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Elastic
Device Class
Class I
Regulation Number
880.5075
Review Panel
HO
Submission Type