VKG 2000 VIDEO KERATOMETER— 510(k) K893968

Substantially Equivalent

Technitex, Inc.

FDA 510(k) clearance K893968 for VKG 2000 VIDEO KERATOMETER, Substantially Equivalent on 1989-09-11. Applicant: Technitex, Inc.. Device class: 1.

Clearance details

Applicant: Technitex, Inc.
Product code: Code HJA
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1989-06-02
Decision date: 1989-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HJA

K901523 — VKG 1000, VIDEO KERATOGRAPH1990-06-27
K842128 — AMERICAN MEDICAL OPTICS PHOTOKERATO1984-08-07
K830290 — DORC CONTACT/PHOTO DERATOSCOPE1983-03-09
K781650 — TERRY KERATOMETER1978-10-17

More clearances from Technitex, Inc.

K883471 — VKG 1000, VIDEO KERATOMETER1988-11-08
K882902 — QRK 100, QUALITATIVE RING KERATOSCOPE1988-08-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.