MARK IV FLOATATION THERAPY BED— 510(k) K901890

Substantially Equivalent

Hydrothermic Floatation Systems, Inc.

FDA 510(k) clearance K901890 for MARK IV FLOATATION THERAPY BED, Substantially Equivalent on 1990-05-07. Applicant: Hydrothermic Floatation Systems, Inc..

Clearance details

Applicant: Hydrothermic Floatation Systems, Inc.
Product code: Code IOQ
Advisory panel: Physical Medicine
Date received: 1990-04-26
Decision date: 1990-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.