The following data is part of a premarket notification filed by Pegasus Research Corp. with the FDA for Pmh 1000 Heated Humidifier.
Device ID | K013856 |
510k Number | K013856 |
Device Name: | PMH 1000 HEATED HUMIDIFIER |
Classification | Humidifier, Respiratory Gas, (direct Patient Interface) |
Applicant | PEGASUS RESEARCH CORP. 1714 SOUTH LYON ST. Santa Ana, CA 92705 |
Contact | Kenneth G Miller |
Correspondent | Kenneth G Miller PEGASUS RESEARCH CORP. 1714 SOUTH LYON ST. Santa Ana, CA 92705 |
Product Code | BTT |
CFR Regulation Number | 868.5450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-06 |
Decision Date | 2003-02-21 |