510(k) K954225

MED-TEC HAND GRIP by Medtec, Inc. — Product Code IXQ

K954225 is an FDA 510(k) premarket notification submitted by Medtec, Inc. for the device "MED-TEC HAND GRIP". The FDA issued a decision of Substantially Equivalent on November 14, 1995. The device falls under product code IXQ (Table, Radiographic, Stationary Top), a Class II device regulated under 21 CFR 892.1980. Medtec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 1995
Date Received
September 11, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Radiographic, Stationary Top
Device Class
Class II
Regulation Number
892.1980
Review Panel
RA
Submission Type