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 |