510(k) K896129

URINARY LEG BAG by Cypress Medical Products, Ltd. — Product Code FAQ

K896129 is an FDA 510(k) premarket notification submitted by Cypress Medical Products, Ltd. for the device "URINARY LEG BAG". The FDA issued a decision of Substantially Equivalent on April 16, 1990. 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. Cypress Medical Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 1990
Date Received
October 23, 1989
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