510(k) K910584

ONE STEP BUTTON(TM) by Applied Medical Technologies — Product Code KGC

K910584 is an FDA 510(k) premarket notification submitted by Applied Medical Technologies for the device "ONE STEP BUTTON(TM)". The FDA issued a decision of Substantially Equivalent on May 23, 1991. The device falls under product code KGC (Tube, Gastro-Enterostomy), a Class II device regulated under 21 CFR 876.5980. Applied Medical Technologies has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 23, 1991
Date Received
February 11, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tube, Gastro-Enterostomy
Device Class
Class II
Regulation Number
876.5980
Review Panel
GU
Submission Type