The following data is part of a premarket notification filed by Merit Medical Systems, Inc. with the FDA for Merit Hi-flex(tm).
| Device ID | K883718 |
| 510k Number | K883718 |
| Device Name: | MERIT HI-FLEX(TM) |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | MERIT MEDICAL SYSTEMS, INC. 79 WEST 4500 SOUTH SUITE 9 Salt Lake City, UT 84107 |
| Contact | P Lampropoulos |
| Correspondent | P Lampropoulos MERIT MEDICAL SYSTEMS, INC. 79 WEST 4500 SOUTH SUITE 9 Salt Lake City, UT 84107 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-31 |
| Decision Date | 1989-01-30 |