FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DIGITAL RADIATION DETECTOR
K Number: K771301
·
Decision Aug 4, 1977
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
29
Applicant Total
4
Review Days
20
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Basic Information
- Device Name
- DIGITAL RADIATION DETECTOR
- K Number
- K771301
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1320
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Actus, Inc.
- Date Received
- July 15, 1977
- Decision Date
- August 4, 1977
- Product Code
- IZD
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| IZD | Probe, Uptake, Nuclear | FDA class 1 | Radiology |
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