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 | Device Class | Medical Specialty |
|---|---|---|---|
| ILO | Pack, Hot Or Cold, Water Circulating | FDA class 2 | Physical Medicine |
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Other Clearances by Breg, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K183702 | Polar Care Wave | Mar 1, 2019 | Substantially Equivalent |
| K041714 | E-PAIN CARE | Oct 1, 2004 | Substantially Equivalent |
| K020988 | PAIN CARE 4200 | Apr 4, 2002 | Substantially Equivalent |
| K013928 | PAIN CARE 3200 | Dec 3, 2001 | Substantially Equivalent |
| K003611 | PAIN CARE MULTI-PORT CATHETER, MODEL 2000L | Dec 13, 2000 | Substantially Equivalent |
| K002073 | PAIN CARE 3000 | Sep 19, 2000 | Substantially Equivalent |
| K002321 | PAIN CARE 2000L | Aug 14, 2000 | Substantially Equivalent |
| K983454 | PAIN CARE 2000 | Dec 16, 1998 | Substantially Equivalent |
| K963596 | POLAR CARE 300 | Dec 4, 1996 | Substantially Equivalent |
| K961855 | POLAR CARE (MODEL 500/50000) | Aug 9, 1996 | Substantially Equivalent |