510(k) K854821

MMG EXTERNAL FEMALE CATHETERS by Medical Technologies of Georgia — Product Code KNX

K854821 is an FDA 510(k) premarket notification submitted by Medical Technologies of Georgia for the device "MMG EXTERNAL FEMALE CATHETERS". The FDA issued a decision of Substantially Equivalent on April 24, 1986. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Medical Technologies of Georgia has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 24, 1986
Date Received
December 3, 1985
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