The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Double Ended Vented Transfer Device.
| Device ID | K801108 |
| 510k Number | K801108 |
| Device Name: | DOUBLE ENDED VENTED TRANSFER DEVICE |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-09 |
| Decision Date | 1980-05-30 |