510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K983606Substantially Equivalent

Is Borrelia Burgdorferi Igm Test System

Columbia Bioscience, Inc., Columbia MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983606 is the FDA 510(k) clearance record for IS BORRELIA BURGDORFERI IGM TEST SYSTEM, a class II device, cleared for Columbia Bioscience, Inc. on under FDA product code LSR (Reagent, Borrelia Serological Reagent). FDA records list 13 510(k) clearances for Columbia Bioscience, Inc., from to . As of , FDA records show no recalls naming K983606.

Clearance record

Decision date
Received
(63 days to decision)
Product code
LSR Reagent, Borrelia Serological Reagent
Regulation
21 CFR 866.3830
Device class
Class II
Review panel
Microbiology
Applicant
Columbia Bioscience, Inc. 8775 M Centre Park Dr., Columbia MD
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