The following data is part of a premarket notification filed by Galt Medical Corp. with the FDA for Catheter Introducer.
Device ID | K043525 |
510k Number | K043525 |
Device Name: | CATHETER INTRODUCER |
Classification | Introducer, Catheter |
Applicant | GALT MEDICAL CORP. 2475 MERRITT DR. Garland, TX 75041 |
Contact | David Catlin |
Correspondent | David Catlin GALT MEDICAL CORP. 2475 MERRITT DR. Garland, TX 75041 |
Product Code | DYB |
CFR Regulation Number | 870.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-12-21 |
Decision Date | 2005-02-09 |
Summary: | summary |