VKG 1000, VIDEO KERATOGRAPH— 510(k) K901523

Substantially Equivalent

The Sanborn Co.

FDA 510(k) clearance K901523 for VKG 1000, VIDEO KERATOGRAPH, Substantially Equivalent on 1990-06-27. Applicant: The Sanborn Co.. Device class: 1.

Clearance details

Applicant: The Sanborn Co.
Product code: Code HJA
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1990-04-02
Decision date: 1990-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HJA

K893968 — VKG 2000 VIDEO KERATOMETER1989-09-11
K842128 — AMERICAN MEDICAL OPTICS PHOTOKERATO1984-08-07
K830290 — DORC CONTACT/PHOTO DERATOSCOPE1983-03-09
K781650 — TERRY KERATOMETER1978-10-17

More clearances from The Sanborn Co.

K901553 — SURG-K SURGICAL KERATOMETER1990-07-20

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