The following data is part of a premarket notification filed by Ventlab Corp. with the FDA for V*care Manual Resuscitator.
Device ID | K012842 |
510k Number | K012842 |
Device Name: | V*CARE MANUAL RESUSCITATOR |
Classification | Ventilator, Emergency, Manual (resuscitator) |
Applicant | VENTLAB CORP. 2934 HWY. 601 NORTH Mocksville, NC 27028 |
Contact | Marge Walls-walker |
Correspondent | Marge Walls-walker VENTLAB CORP. 2934 HWY. 601 NORTH Mocksville, NC 27028 |
Product Code | BTM |
CFR Regulation Number | 868.5915 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-08-23 |
Decision Date | 2001-09-18 |