The following data is part of a premarket notification filed by Medcomp with the FDA for Medcomp Vascu-sheath Introducer Set.
Device ID | K022513 |
510k Number | K022513 |
Device Name: | MEDCOMP VASCU-SHEATH INTRODUCER SET |
Classification | Introducer, Catheter |
Applicant | MEDCOMP 1499 DELP DR. Harleysville, PA 19438 |
Contact | Florence A Caikoski |
Correspondent | Florence A Caikoski MEDCOMP 1499 DELP DR. Harleysville, PA 19438 |
Product Code | DYB |
CFR Regulation Number | 870.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-07-30 |
Decision Date | 2002-10-25 |
Summary: | summary |