510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K812180Substantially Equivalent

Life-Tech #5102 Visulab

Life-Tech Instruments, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812180 is the FDA 510(k) clearance record for LIFE-TECH #5102 VISULAB, a class II device, cleared for Life-Tech Instruments, Inc. on under FDA product code GWN (Nystagmograph). FDA records list 19 510(k) clearances for Life-Tech Instruments, Inc., from to . As of , FDA records show no recalls naming K812180.

Clearance record

Decision date
Received
(18 days to decision)
Product code
GWN Nystagmograph
Regulation
21 CFR 882.1460
Device class
Class II
Review panel
Neurology
Applicant
Life-Tech Instruments, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GWN

Trailing 12 months
1 clearance under product code GWN in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260