510(k) K780494

AMIKACIN by Diagnostic Products Corp. — Product Code KLQ

K780494 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "AMIKACIN". The FDA issued a decision of Substantially Equivalent on April 10, 1978. The device falls under product code KLQ (Radioimmunoassay, Amikacin), a Class II device regulated under 21 CFR 862.3035. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 10, 1978
Date Received
March 27, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Amikacin
Device Class
Class II
Regulation Number
862.3035
Review Panel
TX
Submission Type