510(k) K934883
- Device
- 3D VIDEO SYSTEM
- Applicant
- Richard Wolf Medical Instruments Corp.
- 510(k) number
- K934883
- Product code
- FWG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1994-03-07
- Date received
- 1993-10-12
- Regulation
- 878.4160
- Classification name
- Camera, Television, Endoscopic, With Audio
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- N
Applicant Contact#
- Contact
- ROBERT L CASARSA
- Address
- 353 Corporate Woods Pkwy. Vernon Hills IL US 60061 60061
FDA Registration Numbers#
- 3031240334
- 8010573
- 2518897
- 3038284218
- 9611102
- 3007593944
- 3008699634
- 3013011598
- 3039523130
- 3006680097
- 3005527904
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FWG#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K860173 | VIS-2000 VIDEO SYSTEM | Vistek Corp. | 1986-02-07 |