510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K953077Substantially Equivalent

Paragon Cze 2000 Clinical Capillary Electrophoresis System

Beckman Instruments, Inc., Brea CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K953077 is the FDA 510(k) clearance record for PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM, a class I device, cleared for Beckman Instruments, Inc. on under FDA product code CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin). FDA records list 281 510(k) clearances for Beckman Instruments, Inc., from to . As of , FDA records show no recalls naming K953077.

Clearance record

Decision date
Received
(189 days to decision)
Product code
CDF Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Regulation
21 CFR 862.1795
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Beckman Instruments, Inc. 200 S. Kraemer Blvd., Brea CA
510(k) summary
Summary
Third party review
No

Clearances, product code CDF

Trailing 12 months

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

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