VKG 2000 VIDEO KERATOMETER— 510(k) K893968
Substantially EquivalentTechnitex, Inc.
FDA 510(k) clearance K893968 for VKG 2000 VIDEO KERATOMETER, Substantially Equivalent on 1989-09-11. Applicant: Technitex, Inc..
Clearance details
- Applicant
- Technitex, Inc.
- Product code
- Code HJA
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.