510(k) K883225
K883225 is an FDA 510(k) premarket notification submitted by Richard G. Deniro for the device "FLOSSIE". The FDA issued a decision of Substantially Equivalent on August 30, 1988. The device falls under product code JET (Pick, Massaging), a Class I device regulated under 21 CFR 872.6650.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 30, 1988
- Date Received
- August 1, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pick, Massaging
- Device Class
- Class I
- Regulation Number
- 872.6650
- Review Panel
- DE
- Submission Type