510(k) K960217

CPR URINE BAG by Custom Pack Reliability — Product Code FAQ

K960217 is an FDA 510(k) premarket notification submitted by Custom Pack Reliability for the device "CPR URINE BAG". The FDA issued a decision of Substantially Equivalent on March 28, 1996. The device falls under product code FAQ (Bag, Urine Collection, Leg, For External Use, Sterile), a Class I device regulated under 21 CFR 876.5250. Custom Pack Reliability has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1996
Date Received
January 16, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bag, Urine Collection, Leg, For External Use, Sterile
Device Class
Class I
Regulation Number
876.5250
Review Panel
GU
Submission Type