FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MED-TEC HAND GRIP

K Number: K954225 · Decision Nov 14, 1995
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
26
Applicant Total
41
Review Days
64

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Basic Information

Device Name
MED-TEC HAND GRIP
K Number
K954225
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medtec, Inc.
Date Received
September 11, 1995
Decision Date
November 14, 1995
Product Code
IXQ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IXQ Table, Radiographic, Stationary Top

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K093738 MRI PATIENT POSITIONING DEVICES
K974703 CARBON FIBER BREAST BOARD
K974700 MATRIX MT-MX3
K973842 CARBON FIBER CONFORMAL COUCH TOP
K962622 INTRA-ORAL THERMOPLASTIC SHIELD
K955236 GREEN TEC-2100
K954705 ACRYSTEEL BLOCKING TRAY
K954456 THERMOPLASTIC SHIELD
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