510(k) K780042

HYDORRYBUTYRATE DEHYDROGENASE by Beckman Instruments, Inc. — Product Code JMK

K780042 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "HYDORRYBUTYRATE DEHYDROGENASE". The FDA issued a decision of Substantially Equivalent on February 1, 1978. The device falls under product code JMK (Acid, Alpha-Ketobutyric And Nadh (U.V.), Hydroxybutyric Dehydrogenase), a Class I device regulated under 21 CFR 862.1380. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 1978
Date Received
January 9, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Alpha-Ketobutyric And Nadh (U.V.), Hydroxybutyric Dehydrogenase
Device Class
Class I
Regulation Number
862.1380
Review Panel
CH
Submission Type