510(k) K962687

GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM by Nichols Institute Diagnostics — Product Code JQW

K962687 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM". The FDA issued a decision of Substantially Equivalent on March 28, 1997. The device falls under product code JQW (Station, Pipetting And Diluting, For Clinical Use), a Class I device regulated under 21 CFR 862.2750. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1997
Date Received
July 11, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Station, Pipetting And Diluting, For Clinical Use
Device Class
Class I
Regulation Number
862.2750
Review Panel
CH
Submission Type