510(k) K772300
K772300 is an FDA 510(k) premarket notification submitted by Ritter Co. for the device "DENTAL CHAIR, VANGUARD". The FDA issued a decision of Substantially Equivalent on January 3, 1978. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. Ritter Co. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 1978
- Date Received
- December 14, 1977
- 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