510(k) K873690
K873690 is an FDA 510(k) premarket notification submitted by Cedar Surgical, Inc. for the device "CEDAR(TM) PELVIC CUSHION". The FDA issued a decision of Substantially Equivalent on October 26, 1987. The device falls under product code LWG (Surgical Table Cushion), a Class I device regulated under 21 CFR 878.4950. Cedar Surgical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 26, 1987
- Date Received
- September 8, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Surgical Table Cushion
- Device Class
- Class I
- Regulation Number
- 878.4950
- Review Panel
- SU
- Submission Type