510(k) K953077

PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM by Beckman Instruments, Inc. — Product Code CDF

K953077 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM". The FDA issued a decision of Substantially Equivalent on January 5, 1996. The device falls under product code CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin), a Class I device regulated under 21 CFR 862.1795. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 5, 1996
Date Received
June 30, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Device Class
Class I
Regulation Number
862.1795
Review Panel
CH
Submission Type