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Patient Positioning Devices

by Macromedics BV Netherlands 510(k)

510(k) K142420 Product code IYE

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK142420 Date27 Mar 2015ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

510(k) · synced 22 Oct 2026

510(k) Number
FDA Product Code
IYE
Device Class
Class II
Regulation
21 CFR Part 892.5050
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Other devices from Macromedics BV

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Properties & raw data

Show properties, registry sources and raw records

Sources (1)

  • FDA 510(k) K142420 24 fields · synced 22 Oct 2026