510(k) K962687
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