FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MULTICAM I 8X10
K Number: K912341
·
Decision Aug 26, 1991
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
16
Review Days
94
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Basic Information
- Device Name
- MULTICAM I 8X10
- K Number
- K912341
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Camtronics, Ltd.
- Date Received
- May 24, 1991
- Decision Date
- August 26, 1991
- Product Code
- JAA
- 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 |
|---|---|---|---|
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified | FDA class 2 | Radiology |
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Other Clearances by Camtronics, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K021236 | SURGERY AND ACCESSORIES | Jul 17, 2002 | Substantially Equivalent |
| K013032 | PHYSIOLOG, SERIES 95000 | Jun 4, 2002 | Substantially Equivalent |
| K992666 | VIDEO PLUS SYSTEM, SERIES 95000 | Oct 13, 1999 | Substantially Equivalent |
| K992259 | ECHOCARDIOGRAPHY SYSTEM SERIES 95000 | Sep 8, 1999 | Substantially Equivalent |
| K990066 | CCD CAMERA, MODEL 9000 | Mar 17, 1999 | Substantially Equivalent |
| K955519 | ANALYTICAL REVIEW STATION | May 9, 1996 | Substantially Equivalent |
| K954159 | DIGITAL IMAGING SYSTEM | Mar 19, 1996 | Substantially Equivalent |
| K955232 | NT SERIES DIGITAL IMAGE MANAGER | Dec 11, 1995 | Substantially Equivalent |
| K953080 | DIGITAL IMAGING SYSTEM INTERFACE | Sep 28, 1995 | Substantially Equivalent |
| K945654 | NICOM DIGITAL IMAGE MANAGER | Feb 17, 1995 | Substantially Equivalent |