FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WELL TYPE GAMMA COUNTER
K Number: K771612
·
Decision Apr 10, 1978
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
62
Applicant Total
4
Review Days
230
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Basic Information
- Device Name
- WELL TYPE GAMMA COUNTER
- K Number
- K771612
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2320
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Actus, Inc.
- Date Received
- August 23, 1977
- Decision Date
- April 10, 1978
- Product Code
- JJJ
- Advisory Committee
- Clinical Chemistry
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| JJJ | Counter (Beta, Gamma) For Clinical Use | FDA class 1 | Clinical Chemistry |
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