510(k) K993138

BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT by Ballard Medical Products — Product Code KNT

K993138 is an FDA 510(k) premarket notification submitted by Ballard Medical Products for the device "BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT". The FDA issued a decision of Substantially Equivalent on October 20, 1999. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Ballard Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1999
Date Received
September 20, 1999
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tubes, Gastrointestinal (And Accessories)
Device Class
Class II
Regulation Number
876.5980
Review Panel
GU
Submission Type