510(k) K780251

NEPHELOMETER by Kallestad Laboratories, Inc. — Product Code JQX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 6, 1978
Date Received
February 14, 1978
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