The following data is part of a premarket notification filed by Smiths Medical Md, Inc. with the FDA for Smith Medical Peel-away Sheath Introducers.
Device ID | K112407 |
510k Number | K112407 |
Device Name: | SMITH MEDICAL PEEL-AWAY SHEATH INTRODUCERS |
Classification | Introducer, Catheter |
Applicant | SMITHS MEDICAL MD, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Contact | Tom Bliss |
Correspondent | Tom Bliss SMITHS MEDICAL MD, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Product Code | DYB |
CFR Regulation Number | 870.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-22 |
Decision Date | 2012-02-09 |
Summary: | summary |