510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K922332Substantially Equivalent

Bartels Epstein-Barr Virus Igg Eia

Baxter Diagnostics, Inc., Bellevue WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922332 is the FDA 510(k) clearance record for BARTELS EPSTEIN-BARR VIRUS IGG EIA, a class I device, cleared for Baxter Diagnostics, Inc. on under FDA product code LSE (Epstein-Barr Virus, Other). FDA records list 72 510(k) clearances for Baxter Diagnostics, Inc., from to . As of , FDA records show no recalls naming K922332.

Clearance record

Decision date
Received
(112 days to decision)
Product code
LSE Epstein-Barr Virus, Other
Regulation
21 CFR 866.3235
Device class
Class I
Review panel
Microbiology
Applicant
Baxter Diagnostics, Inc. Bartels Diagnostics Division, Bellevue WA
510(k) summary
Summary
Third party review
No

Clearances, product code LSE

Trailing 12 months
2 clearances under product code LSE in the twelve months to November 2026, October 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LSE, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20262
November 20260