The following data is part of a premarket notification filed by Chad Therapeutics, Inc. with the FDA for Chad Therapeutics Lotus, Models Om-700 And Om-700s.
| Device ID | K042142 |
| 510k Number | K042142 |
| Device Name: | CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S |
| 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 | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-08-09 |
| Decision Date | 2004-09-20 |
| Summary: | summary |