510(k) K925119
K925119 is an FDA 510(k) premarket notification submitted by A-Dec, Inc. for the device "A-DEC 1040 CHAIR". The FDA issued a decision of Substantially Equivalent on January 31, 1994. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. A-Dec, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 31, 1994
- Date Received
- October 9, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chair, Dental, With Operative Unit
- Device Class
- Class I
- Regulation Number
- 872.6250
- Review Panel
- DE
- Submission Type