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

MODIFICATION TO POLAR CARE 500

K Number: K070402 · Decision Mar 29, 2007
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
16
Review Days
45

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Basic Information

Device Name
MODIFICATION TO POLAR CARE 500
K Number
K070402
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Breg, Inc.
Date Received
February 12, 2007
Decision Date
March 29, 2007
Product Code
ILO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ILO Pack, Hot Or Cold, Water Circulating

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Other Clearances by Breg, Inc.

K Number Device Name
K183702 Polar Care Wave
K041714 E-PAIN CARE
K020988 PAIN CARE 4200
K013928 PAIN CARE 3200
K003611 PAIN CARE MULTI-PORT CATHETER, MODEL 2000L
K002073 PAIN CARE 3000
K002321 PAIN CARE 2000L
K983454 PAIN CARE 2000
K963596 POLAR CARE 300
K961855 POLAR CARE (MODEL 500/50000)
Search all 16 clearances from Breg, Inc. →