510(k) K993697
K993697 is an FDA 510(k) premarket notification submitted by Wallac OY for the device "DELFIA NEONATAL IRT KIT". The FDA issued a decision of Substantially Equivalent on June 9, 2000. The device falls under product code CGZ (Electrode, Ion-Specific, Chloride), a Class II device regulated under 21 CFR 862.1170. Wallac OY has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 9, 2000
- Date Received
- November 2, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Ion-Specific, Chloride
- Device Class
- Class II
- Regulation Number
- 862.1170
- Review Panel
- CH
- Submission Type