510(k) K811902
K811902 is an FDA 510(k) premarket notification submitted by Century Manufacturing Co. for the device "CENTURY BIRTHING CHAIR". The FDA issued a decision of Substantially Equivalent on August 25, 1981. The device falls under product code KNC (Table, Obstetric (And Accessories)), a Class II device regulated under 21 CFR 884.4900. Century Manufacturing Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 25, 1981
- Date Received
- July 1, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Obstetric (And Accessories)
- Device Class
- Class II
- Regulation Number
- 884.4900
- Review Panel
- OB
- Submission Type