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.. Device class: 1.

Clearance details

Applicant: Technitex, Inc.
Product code: Code HLP
Device class: Class 1
Regulation: 21 CFR 886.1880
Advisory panel: Ophthalmic
Date received: 1988-08-16
Decision date: 1988-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLP

K874250 — THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.1988-01-11
K874251 — WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHT1988-01-11

More clearances from Technitex, Inc.

K893968 — VKG 2000 VIDEO KERATOMETER1989-09-11
K882902 — QRK 100, QUALITATIVE RING KERATOSCOPE1988-08-04

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