510(k) K922273

ARRAY(R) 360 by Beckman Instruments, Inc. — Product Code JQX

K922273 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "ARRAY(R) 360". The FDA issued a decision of Substantially Equivalent on August 19, 1992. The device falls under product code JQX (Nephelometer, For Clinical Use), a Class I device regulated under 21 CFR 862.2700. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1992
Date Received
May 14, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nephelometer, For Clinical Use
Device Class
Class I
Regulation Number
862.2700
Review Panel
CH
Submission Type