The following data is part of a premarket notification filed by Medimop Medical Projects, Ltd. with the FDA for Vented Vial Adapter Transfer Device.
| Device ID | K062482 |
| 510k Number | K062482 |
| Device Name: | VENTED VIAL ADAPTER TRANSFER DEVICE |
| Classification | Set, I.v. Fluid Transfer |
| Applicant | MEDIMOP MEDICAL PROJECTS, LTD. 17 HAYETZIRA ST. P.O. BOX 2499 Raanana, IL 43665 |
| Contact | Ari Y Sobel |
| Correspondent | Ari Y Sobel MEDIMOP MEDICAL PROJECTS, LTD. 17 HAYETZIRA ST. P.O. BOX 2499 Raanana, IL 43665 |
| Product Code | LHI |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-24 |
| Decision Date | 2006-11-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 27290108241123 | K062482 | 000 |
| 27290108240898 | K062482 | 000 |
| 27290108240751 | K062482 | 000 |
| 27290108240621 | K062482 | 000 |
| 27290108240362 | K062482 | 000 |
| 27290108240126 | K062482 | 000 |
| 27290108240119 | K062482 | 000 |
| 17290108241331 | K062482 | 000 |