510(k) K950029

5STRATEC SL 300 LIA-MAT by Nichols Institute Diagnostics — Product Code JJQ

K950029 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "5STRATEC SL 300 LIA-MAT". The FDA issued a decision of Substantially Equivalent on August 2, 1995. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 2, 1995
Date Received
January 4, 1995
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