510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K761234Substantially Equivalent

Behring Laser Nephelometer

Behring Diagnostics, Inc., San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K761234 is the FDA 510(k) clearance record for BEHRING LASER NEPHELOMETER, a class I device, cleared for Behring Diagnostics, Inc. on under FDA product code JZW (Nephelometer). FDA records list 145 510(k) clearances for Behring Diagnostics, Inc., from to . As of , FDA records show no recalls naming K761234.

Clearance record

Decision date
Received
(0 days to decision)
Product code
JZW Nephelometer
Regulation
21 CFR 866.4540
Device class
Class I
Review panel
Immunology
Applicant
Behring Diagnostics, Inc. 3403 Yerba Buena Rd., San Jose CA
Third party review
No

Clearances, product code JZW

Trailing 12 months

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

FDA records show no clearances under product code JZW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JZW, 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