NURSE'S AID PATIENT ROTATION SYSTEM— 510(k) K973624

Name: FDA 510(k) clearance K973624
Creator: U.S. Food and Drug Administration
Published: 1998-01-21

Substantially Equivalent

Air Med Assist Products

FDA 510(k) clearance K973624 for NURSE'S AID PATIENT ROTATION SYSTEM, Substantially Equivalent on 1998-01-21. Applicant: Air Med Assist Products. Device class: 2.

Clearance details

Applicant: Air Med Assist Products
Product code: Code IOQ
Device class: Class 2
Regulation: 21 CFR 890.5170
Advisory panel: Physical Medicine
Date received: 1997-09-23
Decision date: 1998-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toole, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOQ

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K143414 — Hill-Rom Wireless Connectivity Module2015-03-10
K122473 — TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO22013-06-03
K970363 — HYDROTEC LOW AIR LOSS THERAPY BED1997-11-17
K970364 — AIRTEC2 LOW AIR LOSS THERAPY BED1997-11-17
K970636 — TOTALCARE., MODULAR THERAPY SYSTEM (MTS)1997-08-26

Adverse events under product code IOQ

product code IOQ

Malfunction: 676
Other: 5
Total: 681

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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