The following data is part of a premarket notification filed by Bear Medical Systems, Inc. with the FDA for Penlon Anesthesia Ventilator Series 300.
| Device ID | K842363 |
| 510k Number | K842363 |
| Device Name: | PENLON ANESTHESIA VENTILATOR SERIES 300 |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | BEAR MEDICAL SYSTEMS, 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 | 1984-06-15 |
| Decision Date | 1984-06-26 |