510(k) K853480
K853480 is an FDA 510(k) premarket notification submitted by Skytron, Div. the Kmw Group, Inc. for the device "SKYTRON ELITE 6000 & 6001 SURGICAL TABLES". The FDA issued a decision of Substantially Equivalent on September 12, 1985. The device falls under product code GDC (Table, Operating-Room, Electrical), a Class I device regulated under 21 CFR 878.4960. Skytron, Div. the Kmw Group, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 12, 1985
- Date Received
- August 20, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Operating-Room, Electrical
- Device Class
- Class I
- Regulation Number
- 878.4960
- Review Panel
- SU
- Submission Type