510(k) K870310
K870310 is an FDA 510(k) premarket notification submitted by China National Medicines & Health Prod. I/E Corp. for the device "VSID MEDICAL THREE-FOLDING BED". The FDA issued a decision of Substantially Equivalent on February 10, 1987. The device falls under product code FNJ (Bed, Manual), a Class I device regulated under 21 CFR 880.5120. China National Medicines & Health Prod. I/E Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 1987
- Date Received
- January 28, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bed, Manual
- Device Class
- Class I
- Regulation Number
- 880.5120
- Review Panel
- HO
- Submission Type