FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇰 Denmark
AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849
K Number: K852502
·
Decision Oct 23, 1986
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
4
Review Days
498
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Basic Information
- Device Name
- AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849
- K Number
- K852502
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Bruel & Kjaer Industri A/S
- Date Received
- June 12, 1985
- Decision Date
- October 23, 1986
- Product Code
- IYO
- 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 |
|---|---|---|---|
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | FDA class 2 | Radiology |
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