Class Class II
V80 Anesthetic Vaporizer (V80) (K240375)
Description
V80 Anesthetic Vaporizer (V80) by Shenzhen Mindray Bio-Medical Electronics Co., Ltd., an FDA 510(k) cleared anesthesiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240375
Clearance Date2024-10-31
Clearance TypeTraditional
Product CodeCAD
Regulation Number868.5880
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240375
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. V80 Anesthetic Vaporizer (V80) (K240375) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K150167 | V60 Anesthetic Vaporizer | Shenzhen Mindray Bio-Medical Electr... | 2015 |
| K042276 | D-VAPOR | Draeger Medical, Inc. | 2004 |
Trace the full predicate network for K240375
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.