MJ NEONATAL PERCUSSOR— 510(k) K812151
Substantially EquivalentCussionair Therapy Products, Inc.
FDA 510(k) clearance K812151 for MJ NEONATAL PERCUSSOR, Substantially Equivalent on 1981-08-25. Applicant: Cussionair Therapy Products, Inc..
Clearance details
- Applicant
- Cussionair Therapy Products, Inc.
- Product code
- Code BYI
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Adverse events under product code BYI
product code BYI- Death
- 3
- Total
- 3
Source: openFDA MAUDE database, through . 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.