The following data is part of a premarket notification filed by Nihon Kohden America, Inc. with the FDA for Lifescope 6, Oec-6120 Portable Patient Monitor Rec.
| Device ID | K862462 |
| 510k Number | K862462 |
| Device Name: | LIFESCOPE 6, OEC-6120 PORTABLE PATIENT MONITOR REC |
| Classification | Monitor, Breathing Frequency |
| Applicant | NIHON KOHDEN AMERICA, INC. 17112 ARMSTRONG AVE. Irvine, CA 92714 |
| Contact | Dennis Javens |
| Correspondent | Dennis Javens NIHON KOHDEN AMERICA, INC. 17112 ARMSTRONG AVE. Irvine, CA 92714 |
| Product Code | BZQ |
| CFR Regulation Number | 868.2375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-06-30 |
| Decision Date | 1987-02-03 |