The following data is part of a premarket notification filed by Emerson-sack-warner Corp. with the FDA for Table, Operating, Field 6530-00-709-8175.
| Device ID | K821923 |
| 510k Number | K821923 |
| Device Name: | TABLE, OPERATING, FIELD 6530-00-709-8175 |
| Classification | Table, Operating-room, Mechanical |
| Applicant | EMERSON-SACK-WARNER CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FWX |
| CFR Regulation Number | 878.4950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-29 |
| Decision Date | 1982-07-13 |