510(k) K792045

BIOVATION NEPHELOMETER by Biovation, Inc. — Product Code JQX

K792045 is an FDA 510(k) premarket notification submitted by Biovation, Inc. for the device "BIOVATION NEPHELOMETER". The FDA issued a decision of Substantially Equivalent on October 30, 1979. The device falls under product code JQX (Nephelometer, For Clinical Use), a Class I device regulated under 21 CFR 862.2700. Biovation, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1979
Date Received
October 12, 1979
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