The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Adapters-y-type.
| Device ID | K790563 |
| 510k Number | K790563 |
| Device Name: | ADAPTERS-Y-TYPE |
| Classification | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
| Applicant | DLP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTL |
| CFR Regulation Number | 870.4290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-03-19 |
| Decision Date | 1979-04-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00643169767676 | K790563 | 000 |
| 20613994736660 | K790563 | 000 |
| 20613994736769 | K790563 | 000 |
| 20613994736783 | K790563 | 000 |
| 20613994756057 | K790563 | 000 |
| 20613994808022 | K790563 | 000 |
| 20613994808046 | K790563 | 000 |
| 20613994808060 | K790563 | 000 |
| 00673978861395 | K790563 | 000 |
| 20613994736653 | K790563 | 000 |