The following data is part of a premarket notification filed by Terumo Medical Corp. with the FDA for Glidesheath.
| Device ID | K082644 |
| 510k Number | K082644 |
| Device Name: | GLIDESHEATH |
| Classification | Introducer, Catheter |
| Applicant | TERUMO MEDICAL CORP. 950 Elkton Blvd. Elkton, MD 21921 |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2008-09-11 |
| Decision Date | 2008-09-18 |
| Summary: | summary |