STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500— 510(k) K920526

Name: FDA 510(k) clearance K920526
Creator: U.S. Food and Drug Administration
Published: 1992-09-21

Substantially Equivalent

Stryker Medical

FDA 510(k) clearance K920526 for STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500, Substantially Equivalent on 1992-09-21. Applicant: Stryker Medical. Device class: 1.

Clearance details

Applicant: Stryker Medical
Product code: Code IOG
Device class: Class 1
Regulation: 21 CFR 890.5370
Advisory panel: Physical Medicine
Date received: 1992-02-04
Decision date: 1992-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOG

view all

K801250 — HYDRA TRED DC1980-06-17
K800251 — MT-10, ET-201980-04-02

More clearances from Stryker Medical

view all

K222818 — Xpedition Powered Stair Chair (625700000000)2023-01-24
K180834 — Altrix Precision Temperature Management System2018-08-10
K171149 — Altrix Temperature Management Wraps2017-07-18
K152266 — Altrix Precision Temperature Management System2016-12-02
K113598 — POWER-LOAD COT FASTENER SYSTEM2011-12-20

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