510(k) K822307

ADHESIVE SPRAY #4050-4060 by The Healthcare Group Laboratories, Inc. — Product Code KNX

K822307 is an FDA 510(k) premarket notification submitted by The Healthcare Group Laboratories, Inc. for the device "ADHESIVE SPRAY #4050-4060". The FDA issued a decision of Substantially Equivalent on September 24, 1982. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. The Healthcare Group Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 1982
Date Received
August 3, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Collector, Urine, (And Accessories) For Indwelling Catheter
Device Class
Class II
Regulation Number
876.5250
Review Panel
GU
Submission Type