MARK 5 NUVO OCSI (M5C5), MODELS 505 AND 905— 510(k) K040892
Substantially EquivalentNidek Medical Products, Inc.
FDA 510(k) clearance K040892 for MARK 5 NUVO OCSI (M5C5), MODELS 505 AND 905, Substantially Equivalent on 2004-04-29. Applicant: Nidek Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Nidek Medical Products, Inc.
- Product code
- Code CAW
- Device class
- Class 2
- Regulation
- 21 CFR 868.5440
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Birmingham, AL, US
Recent devices under product code CAW
view allMore clearances from Nidek Medical Products, Inc.
view allAdverse events under product code CAW
product code CAW- Death
- 204
- Injury
- 573
- Malfunction
- 1,400
- Other
- 6
- Total
- 2,183
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.