IMMOBILIZING VACUUM MATRESS (IVM)— 510(k) K863511

Name: FDA 510(k) clearance K863511
Creator: U.S. Food and Drug Administration
Published: 1986-09-25

Substantially Equivalent

Omnium Services Partners, Inc.

FDA 510(k) clearance K863511 for IMMOBILIZING VACUUM MATRESS (IVM), Substantially Equivalent on 1986-09-25. Applicant: Omnium Services Partners, Inc.. Device class: 1.

Clearance details

Applicant: Omnium Services Partners, Inc.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1986-09-09
Decision date: 1986-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winter Park, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FPP

view all

K030283 — BABY POD2003-04-22
K942356 — MED-EVAC-4 MEDICAL EVACUATION STRETCHER1994-07-19
K940130 — STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER1994-03-10
K940245 — EVACU-SLED1994-02-28
K924275 — RESTRAINING STRETCHER1993-07-27

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