The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Multi-ad Fluid Dispensing Pump Mp-3000.
| Device ID | K801008 |
| 510k Number | K801008 |
| Device Name: | MULTI-AD FLUID DISPENSING PUMP MP-3000 |
| Classification | Dispenser, Liquid Medication |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KYX |
| CFR Regulation Number | 880.6430 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-04-28 |
| Decision Date | 1980-06-02 |