Devon Cirona 6100 Dvt

by Devon Medical, Inc. 510(k)

Active United States

510(k) K130571

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK130571	Date9 Apr 2013Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K130571
FDA Product Code: JOW

Device Class: Class II
Regulation: 21 CFR Part 870.5800
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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