The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Pole, Intravenous.
| Device ID | K880537 |
| 510k Number | K880537 |
| Device Name: | POLE, INTRAVENOUS |
| Classification | Stand, Infusion |
| Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Contact | Frank Ferguson |
| Correspondent | Frank Ferguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Product Code | FOX |
| CFR Regulation Number | 880.6990 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-09 |
| Decision Date | 1988-04-06 |