510(k) K952815

DUPONT LIPASE CALIBRATOR by Dupont Medical Products — Product Code JIT

K952815 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "DUPONT LIPASE CALIBRATOR". The FDA issued a decision of Substantially Equivalent on August 31, 1995. The device falls under product code JIT (Calibrator, Secondary), a Class II device regulated under 21 CFR 862.1150. Dupont Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 31, 1995
Date Received
June 20, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator, Secondary
Device Class
Class II
Regulation Number
862.1150
Review Panel
CH
Submission Type