The following data is part of a premarket notification filed by Gish Biomedical, Inc. with the FDA for Medos Hilite Oxygenator, Model 7000 & 7000 Lt.
| Device ID | K082403 |
| 510k Number | K082403 |
| Device Name: | MEDOS HILITE OXYGENATOR, MODEL 7000 & 7000 LT |
| Classification | Oxygenator, Cardiopulmonary Bypass |
| Applicant | GISH BIOMEDICAL, INC. 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 |
| Contact | Harvey Knauss |
| Correspondent | Harvey Knauss GISH BIOMEDICAL, INC. 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 |
| Product Code | DTZ |
| CFR Regulation Number | 870.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-21 |
| Decision Date | 2009-05-15 |
| Summary: | summary |