SYSTEM 3000 FLUIDIZED AIR BED— 510(k) K890935

Name: FDA 510(k) clearance K890935
Creator: U.S. Food and Drug Administration
Published: 1989-03-15

Substantially Equivalent

Dermanetics Corp.

FDA 510(k) clearance K890935 for SYSTEM 3000 FLUIDIZED AIR BED, Substantially Equivalent on 1989-03-15. Applicant: Dermanetics Corp.. Device class: 2.

Clearance details

Applicant: Dermanetics Corp.
Product code: Code IOQ
Device class: Class 2
Regulation: 21 CFR 890.5170
Advisory panel: Physical Medicine
Date received: 1989-02-24
Decision date: 1989-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Beach, CA, US

Download summary PDF View on FDA.gov ↗

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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.