The following data is part of a premarket notification filed by Terumo Medical Corp. with the FDA for Radifocus Introducer Ii Kit.
| Device ID | K954234 |
| 510k Number | K954234 |
| Device Name: | RADIFOCUS INTRODUCER II KIT |
| Classification | Introducer, Catheter |
| Applicant | TERUMO MEDICAL CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
| Contact | Keith Smith |
| Correspondent | Keith Smith TERUMO MEDICAL CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-09-11 |
| Decision Date | 1995-11-27 |