FDA-recognized standard · Anesthesiology
ISO 10079-3: Medical suction equipment - Part 3: Suction equipment powered from a vacuum or positive pressure gas source
Yes. FDA recognizes ISO 10079-3 Fourth edition 2022-03 as recognition 1-156, entered 2022-12-19.
Recognized editions of ISO 10079-3
| Recognition | Edition | Entered | Extent | Transition ends |
|---|---|---|---|---|
| 1-156 | ISO 10079-3 Fourth edition 2022-03 | 2022-12-19 | Complete | — |
Regulations
FDA lists these classification regulations against ISO 10079-3: 21 CFR 868.6810, 21 CFR 870.5050, 21 CFR 870.5910, 21 CFR 874.5350, 21 CFR 878.4683, 21 CFR 878.4780, 21 CFR 878.5040, 21 CFR 880.6740.
Product codes that cite ISO 10079-3
16 FDA product codes cite ISO 10079-3, including BSY, BTA, CBC, DWM, EWT.
- BSY
- BTA Pump, Portable, Aspiration (Manual Or Powered)
- CBC
- DWM
- EWT
- GCX
- KDP
- KDQ
- MUU System, Suction, Lipoplasty
- OJR
- OKO
- OMP Negative Pressure Wound Therapy Powered Suction Pump
- OTK
- PAD
- PLA
- QPB System, Suction, Lipoplasty For Removal
Source: FDA Recognized Consensus Standards database, snapshot of 2026-09-01. Search every recognition in the Consensus Standards Lookup, or browse all standards with a page.