MOVIT DEVICE— 510(k) K921710
Substantially EquivalentJohn J. Navar, M.D.
FDA 510(k) clearance K921710 for MOVIT DEVICE, Substantially Equivalent on 1992-06-29. Applicant: John J. Navar, M.D.. Device class: 1.
Clearance details
- Applicant
- John J. Navar, M.D.
- Product code
- Code BRY
- Device class
- Class 1
- Regulation
- 21 CFR 868.6100
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Corpus Christi, TX, US
Recent devices under product code BRY
view allAdverse events under product code BRY
product code BRY- Death
- 9
- Malfunction
- 75,890
- Total
- 75,899
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.