The following data is part of a premarket notification filed by Hillwood Corp. with the FDA for Pipettes, Plastic Disposable.
| Device ID | K781891 |
| 510k Number | K781891 |
| Device Name: | PIPETTES, PLASTIC DISPOSABLE |
| Classification | Pipette, Quantitative, Hematology |
| Applicant | HILLWOOD CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GJG |
| CFR Regulation Number | 864.6160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-11-08 |
| Decision Date | 1978-11-15 |