DeviceClearance

MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370— 510(k) K050951

Substantially Equivalent

Cibernet Systems Corp.

FDA 510(k) clearance K050951 for MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370, Substantially Equivalent on 2005-07-19. Applicant: Cibernet Systems Corp.. Device class: 2.

Clearance details

Applicant
Cibernet Systems Corp.
Product code
Code DXH
Device class
Class 2
Regulation
21 CFR 870.2920
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Ann Arbor, MI, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DXH

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Data sourced from openFDA. This site is unofficial and independent of the FDA.