510(k) K791993
K791993 is an FDA 510(k) premarket notification submitted by Skil-Care Corp. for the device "SKIL-CARE BED RAIL PADS". The FDA issued a decision of Substantially Equivalent on October 26, 1979. The device falls under product code FNJ (Bed, Manual), a Class I device regulated under 21 CFR 880.5120. Skil-Care Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 26, 1979
- Date Received
- October 3, 1979
- 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