The following data is part of a premarket notification filed by Chad Therapeutics, Inc. with the FDA for Chad Therapeutics Oxypenumatic Cypress Model 511.
Device ID | K020475 |
510k Number | K020475 |
Device Name: | CHAD THERAPEUTICS OXYPENUMATIC CYPRESS MODEL 511 |
Classification | Conserver, Oxygen |
Applicant | CHAD THERAPEUTICS, INC. 21622 PLUMMER ST. Chatsworth, CA 91311 |
Contact | Kevin Mcculloh |
Correspondent | Kevin Mcculloh CHAD THERAPEUTICS, INC. 21622 PLUMMER ST. Chatsworth, CA 91311 |
Product Code | NFB |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-02-12 |
Decision Date | 2002-07-05 |
Summary: | summary |