The following data is part of a premarket notification filed by Hudson Oxygen Therapy Sales Co. with the FDA for Infant C.p.a.p. Monitor.
Device ID | K896136 |
510k Number | K896136 |
Device Name: | INFANT C.P.A.P. MONITOR |
Classification | Monitor, Airway Pressure (includes Gauge And/or Alarm) |
Applicant | HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula, CA 92390 |
Contact | Jorge Haider |
Correspondent | Jorge Haider HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula, CA 92390 |
Product Code | CAP |
CFR Regulation Number | 868.2600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-10-23 |
Decision Date | 1990-01-09 |