The following data is part of a premarket notification filed by Gainor Medical with the FDA for Gainor Medical Flowmax Needles.
| Device ID | K844305 |
| 510k Number | K844305 |
| Device Name: | GAINOR MEDICAL FLOWMAX NEEDLES |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | GAINOR MEDICAL 12520 YELLOWHEAD TRAIL |
| Contact | Mark Gainor |
| Correspondent | Mark Gainor GAINOR MEDICAL 12520 YELLOWHEAD TRAIL |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-11-06 |
| Decision Date | 1984-11-30 |