510(k) K883471
- Device
- Vkg 1000, Video Keratometer
- Applicant
- TECHNITEX, INC.
- 510(k) number
- K883471
- Product code
- HLP
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1988-11-08
- Date received
- 1988-08-16
- Regulation
- 886.1880
- Classification name
- Target, Fusion And Stereoscopic
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- RICHARD K SNOOK
- Address
- 11211 Richmond Ave., Suite 103 Houston TX US 77082 77082
FDA Registration Numbers#
- 3004950803
- 3008688147
- 1926420
- 3003775438
- 2518410
Source Documents#
510(k) summary PDF not indicated by FDA