VKG 1000, VIDEO KERATOMETER— 510(k) K883471

Substantially Equivalent

Technitex, Inc.

FDA 510(k) clearance K883471 for VKG 1000, VIDEO KERATOMETER, Substantially Equivalent on 1988-11-08. Applicant: Technitex, Inc..

Clearance details

Applicant: Technitex, Inc.
Product code: Code HLP
Advisory panel: Ophthalmic
Date received: 1988-08-16
Decision date: 1988-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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