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

AUTOGEL PAD

K Number: K031018 · Decision Dec 8, 2003
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
33
Applicant Total
43
Review Days
252

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Basic Information

Device Name
AUTOGEL PAD
K Number
K031018
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Rich-Mar Corp.
Date Received
March 31, 2003
Decision Date
December 8, 2003
Product Code
MUI
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
MUI Media, Coupling, Ultrasound

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Other Clearances by Rich-Mar Corp.

K Number Device Name
K040679 RICH-MAR AUTOPRISM INFRARED LAMP
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K021483 RICH-MAR THERASOUND 6.5 THERAPEUTIC ULTRASOUND
K013770 MODIFICATION TO: WINNER ST-2 STIMULATOR
K013771 MODIFICATION TO: WINNER CM-2 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE
K012848 WINNER CM4 COMBINATION UNIT
K000808 RICH-MAR WINNER ST4 MUSCLE STIMULATOR, INTERFERENTIAL, AND TENS DEVICE
K982544 RICH-MAR US500, US750, US1000 THERAPEUTIC UNLTRASOUND DEVICES
K952089 RICH-MAR CM-II COMBINED MUSCLE STIMULATOR, INTERFERENTIAL, TENS & THERAPEUTIC ULTRASOUND DEVICE
K950564 RICH-MAR US-II ULTRASOUND
Search all 43 clearances from Rich-Mar Corp. →