The following data is part of a premarket notification filed by Vortran Medical Technology 1, Inc. with the FDA for Piper Ippb Model 2055.
Device ID | K982016 |
510k Number | K982016 |
Device Name: | PIPER IPPB MODEL 2055 |
Classification | Device, Positive Pressure Breathing, Intermittent |
Applicant | VORTRAN MEDICAL TECHNOLOGY 1, INC. 3941 J ST., SUITE 354 Sacramento, CA 95819 |
Contact | Gordon A Wong |
Correspondent | Gordon A Wong VORTRAN MEDICAL TECHNOLOGY 1, INC. 3941 J ST., SUITE 354 Sacramento, CA 95819 |
Product Code | NHJ |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-06-08 |
Decision Date | 1998-11-03 |