The following data is part of a premarket notification filed by Chad Therapeutics, Inc. with the FDA for Chad Therapeutics Bonsai Model 800.
| Device ID | K070740 |
| 510k Number | K070740 |
| Device Name: | CHAD THERAPEUTICS BONSAI MODEL 800 |
| 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 | 2007-03-16 |
| Decision Date | 2007-05-07 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00822383504322 | K070740 | 000 |
| 00814470020204 | K070740 | 000 |
| 00814470020235 | K070740 | 000 |
| 00814470020242 | K070740 | 000 |
| 00814470020266 | K070740 | 000 |
| 00814470020273 | K070740 | 000 |
| 00814470020297 | K070740 | 000 |
| 00814470020327 | K070740 | 000 |
| 00814470020358 | K070740 | 000 |
| 00814470020037 | K070740 | 000 |