510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071712Substantially Equivalent

Leuko Ez Vue

Techlab Inc., Corporate Research Center, Blacksburg VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071712 is the FDA 510(k) clearance record for LEUKO EZ VUE, a class I device, cleared for Techlab Inc., Corporate Research Center on under FDA product code DEG (Lactoferrin, Antigen, Antiserum, Control). FDA records list 5 510(k) clearances for Techlab Inc., Corporate Research Center, from to . As of , FDA records show no recalls naming K071712.

Clearance record

Decision date
Received
(165 days to decision)
Product code
DEG Lactoferrin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5570
Device class
Class I
Review panel
Immunology
Applicant
Techlab Inc., Corporate Research Center 2001 Kraft Dr., Blacksburg VA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DEG

Trailing 12 months

FDA records hold no clearances under product code DEG in the trailing twelve months.

FDA records show no clearances under product code DEG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DEG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260