The following data is part of a premarket notification filed by Owens-illinois, Inc. with the FDA for Disposable Controlled Drop Pasteur Pipet.
| Device ID | K780237 |
| 510k Number | K780237 |
| Device Name: | DISPOSABLE CONTROLLED DROP PASTEUR PIPET |
| Classification | Pipette, Quantitative, Hematology |
| Applicant | OWENS-ILLINOIS, INC. 19 LEIGH FISHER BLVD. El Paso, TX 79906 |
| Product Code | GJG |
| CFR Regulation Number | 864.6160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-13 |
| Decision Date | 1978-03-09 |