The following data is part of a premarket notification filed by Steris Corporation with the FDA for Steris Cmax Xlt Surgical Table.
| Device ID | K090136 |
| 510k Number | K090136 |
| Device Name: | STERIS CMAX XLT SURGICAL TABLE |
| Classification | Table, Operating-room, Ac-powered |
| Applicant | STERIS Corporation 5960 Heisley Road Mentor, OH 44060 |
| Contact | John Robert Scoville |
| Correspondent | John Robert Scoville STERIS Corporation 5960 Heisley Road Mentor, OH 44060 |
| Product Code | FQO |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-01-21 |
| Decision Date | 2009-03-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00724995202996 | K090136 | 000 |
| 00724995164379 | K090136 | 000 |
| 00724995190590 | K090136 | 000 |
| 00724995191016 | K090136 | 000 |
| 00724995154936 | K090136 | 000 |
| 00724995154943 | K090136 | 000 |
| 00724995154950 | K090136 | 000 |
| 00724995154974 | K090136 | 000 |
| 00724995154981 | K090136 | 000 |
| 00724995154998 | K090136 | 000 |
| 00724995155513 | K090136 | 000 |
| 00724995155520 | K090136 | 000 |
| 00724995155537 | K090136 | 000 |
| 00724995155544 | K090136 | 000 |
| 00724995155551 | K090136 | 000 |
| 00724995202989 | K090136 | 000 |
| 00724995164362 | K090136 | 000 |