510(k) K941050

DUPONT ACA STAR by Dupont Medical Products — Product Code JJQ

K941050 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "DUPONT ACA STAR". The FDA issued a decision of Substantially Equivalent on November 10, 1994. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Dupont Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 10, 1994
Date Received
March 7, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class
Class I
Regulation Number
862.2300
Review Panel
CH
Submission Type