FiAPC plus probes

by Erbe Elektromedizin GmbH 2 variants

510(k) K242044

FiAPC plus probes is a Class II device made by Erbe Elektromedizin GmbH, cleared under FDA 510(k) K242044 on 26 Aug 2024, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K242044↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK242044	Date26 Aug 2024Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K242044

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K242044
FDA product code: GEI

Device class: Class II
Regulation: 21 CFR Part 878.4400
Advisory committee: General, Plastic Surgery
FDA decision: SESE Substantially Equivalent

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