Chad Therapeutics Bonsai Model 800

FDA 510(k) K070740 · Chad Therapeutics, Inc.

Substantially Equivalent

510(k) numberK070740

Submission

Device name
Chad Therapeutics Bonsai Model 800
Applicant
Chad Therapeutics, Inc.
Chatsworth, CA, US
Received
March 16, 2007
Decision date
May 7, 2007
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NFB – Conserver, Oxygen
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5905
Specialty
Anesthesiology

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Questions and answers

When was Chad Therapeutics Bonsai Model 800 cleared by the FDA?

Chad Therapeutics Bonsai Model 800 (K070740) received a 510(k) decision of Substantially Equivalent on May 7, 2007, 52 days after the submission was received.

What is the product code of K070740?

The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.