510(k) K820142

TUBULAR STOCKINETTE by Stan-Pak Ent. — Product Code FQM

K820142 is an FDA 510(k) premarket notification submitted by Stan-Pak Ent. for the device "TUBULAR STOCKINETTE". The FDA issued a decision of Substantially Equivalent on February 5, 1982. The device falls under product code FQM (Bandage, Elastic), a Class I device regulated under 21 CFR 880.5075. Stan-Pak Ent. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 1982
Date Received
January 19, 1982
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