510(k) K822992
K822992 is an FDA 510(k) premarket notification submitted by Convaid Products, Inc. for the device "PEOPLE MOVER". The FDA issued a decision of Substantially Equivalent on October 27, 1982. The device falls under product code INM (Chair, With Casters), a Class I device regulated under 21 CFR 890.3100. Convaid Products, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 1982
- Date Received
- October 12, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chair, With Casters
- Device Class
- Class I
- Regulation Number
- 890.3100
- Review Panel
- PM
- Submission Type