510(k) K832648

ACCLAIM by Electro-Nucleonics Laboratories, Inc. — Product Code JJE

K832648 is an FDA 510(k) premarket notification submitted by Electro-Nucleonics Laboratories, Inc. for the device "ACCLAIM". The FDA issued a decision of Substantially Equivalent on September 20, 1983. The device falls under product code JJE (Analyzer, Chemistry (Photometric, Discrete), For Clinical Use), a Class I device regulated under 21 CFR 862.2160. Electro-Nucleonics Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 20, 1983
Date Received
August 5, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
Device Class
Class I
Regulation Number
862.2160
Review Panel
CH
Submission Type