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Arterial Blood Sampling Kit

FDA product code CBT · 58 cleared devices

Class 1 Anesthesiology
Regulation
21 CFR 868.1100
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1977-07-01 – 2007-08-01

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

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