FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CPR LOCATOR
K Number: K833737
·
Decision Aug 24, 1984
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
16
Applicant Total
3
Review Days
304
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Basic Information
- Device Name
- CPR LOCATOR
- K Number
- K833737
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.5210
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Lifepoint,Inc
- Date Received
- October 25, 1983
- Decision Date
- August 24, 1984
- Product Code
- LIX
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| LIX | Aid, Cardiopulmonary Resuscitation | FDA class 2 | Cardiovascular |
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