510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943812Substantially Equivalent

Vidas Lyme Screen II

Biomerieux Vitek, Inc., Rockland MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943812 is the FDA 510(k) clearance record for VIDAS LYME SCREEN II, a class II device, cleared for Biomerieux Vitek, Inc. on under FDA product code LSR (Reagent, Borrelia Serological Reagent). FDA records list 49 510(k) clearances for Biomerieux Vitek, Inc., from to . As of , FDA records show one recall naming K943812.

Clearance record

Decision date
Received
(312 days to decision)
Product code
LSR Reagent, Borrelia Serological Reagent
Regulation
21 CFR 866.3830
Device class
Class II
Review panel
Microbiology
Applicant
Biomerieux Vitek, Inc. 1022 Hingham St., Rockland MA
510(k) summary
Summary
Third party review
No

Clearances, product code LSR

Trailing 12 months
2 clearances under product code LSR in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LSR, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260