CELLERATION MIST THERAPY SYSTEM 5.1— 510(k) K050129

Substantially Equivalent

Celleration, Inc.

FDA 510(k) clearance K050129 for CELLERATION MIST THERAPY SYSTEM 5.1, Substantially Equivalent on 2005-05-17. Applicant: Celleration, Inc..

Clearance details

Applicant: Celleration, Inc.
Product code: Code NRB
Advisory panel: General, Plastic Surgery
Date received: 2005-01-19
Decision date: 2005-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

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Adverse events under product code NRB

product code NRB

Other: 1
Total: 1

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.