510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K896378Substantially Equivalent

Lyme-Check(tm) Test Kit

Diagnostic Technology, Inc., Hauppauge NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896378 is the FDA 510(k) clearance record for LYME-CHECK(TM) TEST KIT, a class II device, cleared for Diagnostic Technology, Inc. on under FDA product code LSR (Reagent, Borrelia Serological Reagent). FDA records list 28 510(k) clearances for Diagnostic Technology, Inc., from to . As of , FDA records show no recalls naming K896378.

Clearance record

Decision date
Received
(729 days to decision)
Product code
LSR Reagent, Borrelia Serological Reagent
Regulation
21 CFR 866.3830
Device class
Class II
Review panel
Microbiology
Applicant
Diagnostic Technology, Inc. 240 Vanderbilt Motor Pkwy., Hauppauge NY
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