510(k) K892700
K892700 is an FDA 510(k) premarket notification submitted by Rifton Equipment For the Handicapped for the device "E65 35 PRONE STANDER". The FDA issued a decision of Substantially Equivalent on May 9, 1989. The device falls under product code INW (Table, Mechanical), a Class I device regulated under 21 CFR 890.3750. Rifton Equipment For the Handicapped has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 1989
- Date Received
- April 13, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Mechanical
- Device Class
- Class I
- Regulation Number
- 890.3750
- Review Panel
- PM
- Submission Type