The following data is part of a premarket notification filed by Lifecare Services, Inc. with the FDA for Respiraotr, Cam-10 Rbl.
Device ID | K790605 |
510k Number | K790605 |
Device Name: | RESPIRAOTR, CAM-10 RBL |
Classification | Ventilator, Continuous, Facility Use |
Applicant | LIFECARE SERVICES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-03-29 |
Decision Date | 1979-07-03 |