The following data is part of a premarket notification filed by Koven Technology, Inc. with the FDA for Bi-directional Doppler Volume Flowmeter, Model Dvm-4300 & 4300t.
| Device ID | K010452 |
| 510k Number | K010452 |
| Device Name: | BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T |
| Classification | Flowmeter, Blood, Cardiovascular |
| Applicant | KOVEN TECHNOLOGY, INC. 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 -3404 |
| Contact | J. Harvey Knauss |
| Correspondent | J. Harvey Knauss KOVEN TECHNOLOGY, INC. 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 -3404 |
| Product Code | DPW |
| CFR Regulation Number | 870.2100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-02-15 |
| Decision Date | 2002-02-12 |