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ARDO SUCTION PUMP MASTER - Ardo Suction Pump Master, Model 30.00.XX

by Ardo medical AG

510(k) K011601

Listed No authorization on record

Valid until

Not applicable

No authorization on record

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 7 Oct 2026. What this means

Specification

510(k)

510(k) Number
FDA Product Code
BTA
Models / Variants
Ardo Suction Pump Master, Model 30.00.XX
Device Class
Class II
Regulation
21 CFR Part 878.4780
Advisory Committee
General, Plastic Surgery
FDA Decision
SESE Substantially Equivalent

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