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 |