The following data is part of a premarket notification filed by Medimop Medical Projects, Ltd. with the FDA for Mixject With Spray Head.
| Device ID | K122023 |
| 510k Number | K122023 |
| Device Name: | MIXJECT WITH SPRAY HEAD |
| Classification | Syringe, Piston |
| Applicant | MEDIMOP MEDICAL PROJECTS, LTD. 17 HATIDHAR ST. Raanana, IL 43665 |
| Contact | Llanit Goldgraber |
| Correspondent | Llanit Goldgraber MEDIMOP MEDICAL PROJECTS, LTD. 17 HATIDHAR ST. Raanana, IL 43665 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-07-11 |
| Decision Date | 2012-10-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 27290108240935 | K122023 | 000 |