The following data is part of a premarket notification filed by Versamed Medical Systems, Inc. with the FDA for Modification To I Vent 201.
Device ID | K061627 |
510k Number | K061627 |
Device Name: | MODIFICATION TO I VENT 201 |
Classification | Ventilator, Continuous, Facility Use |
Applicant | VERSAMED MEDICAL SYSTEMS, INC. 2 BLUE HILL PLAZA BLDG. 2, 3RD FLOOR Pearl River, NY 10965 |
Contact | Jerry Korten |
Correspondent | Jerry Korten VERSAMED MEDICAL SYSTEMS, INC. 2 BLUE HILL PLAZA BLDG. 2, 3RD FLOOR Pearl River, NY 10965 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-06-12 |
Decision Date | 2006-06-29 |
Summary: | summary |