The following data is part of a premarket notification filed by Bailey Mfg. Co. with the FDA for Pro. Hi-low Treatment Tables Models 4050,4070,4090.
| Device ID | K932237 |
| 510k Number | K932237 |
| Device Name: | PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090 |
| Classification | Table, Powered |
| Applicant | BAILEY MFG. CO. P.O. BOX 130 Lodi, OH 44254 |
| Contact | Thomas Campbell |
| Correspondent | Thomas Campbell BAILEY MFG. CO. P.O. BOX 130 Lodi, OH 44254 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-07 |
| Decision Date | 1993-07-22 |