ULTRAFLOTATION BED— 510(k) K882607

Substantially Equivalent

Medical Flotation Systems, Inc.

FDA 510(k) clearance K882607 for ULTRAFLOTATION BED, Substantially Equivalent on 1988-10-14. Applicant: Medical Flotation Systems, Inc..

Clearance details

Applicant: Medical Flotation Systems, Inc.
Product code: Code IOQ
Advisory panel: Physical Medicine
Date received: 1988-06-24
Decision date: 1988-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

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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.