510(k) K960245
K960245 is an FDA 510(k) premarket notification submitted by Pro-Dentec for the device "VIP VICTOR INTERACTIVE PROBE". The FDA issued a decision of Substantially Equivalent on April 4, 1996. The device falls under product code EIX (Probe, Periodontic), a Class I device regulated under 21 CFR 872.4565. Pro-Dentec has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 4, 1996
- Date Received
- January 16, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Probe, Periodontic
- Device Class
- Class I
- Regulation Number
- 872.4565
- Review Panel
- DE
- Submission Type