510(k) K863244

AMIKACIN (FPIA) CALIBRATOR KIT by Windsor Laboratories, Inc. — Product Code DLJ

K863244 is an FDA 510(k) premarket notification submitted by Windsor Laboratories, Inc. for the device "AMIKACIN (FPIA) CALIBRATOR KIT". The FDA issued a decision of Substantially Equivalent on August 29, 1986. The device falls under product code DLJ (Calibrators, Drug Specific), a Class II device regulated under 21 CFR 862.3200. Windsor Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1986
Date Received
August 22, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrators, Drug Specific
Device Class
Class II
Regulation Number
862.3200
Review Panel
TX
Submission Type