MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000— 510(k) K001106
Substantially EquivalentCreative Plastic Technology
FDA 510(k) clearance K001106 for MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000, Substantially Equivalent on 2000-08-16. Applicant: Creative Plastic Technology.
Clearance details
- Applicant
- Creative Plastic Technology
- Product code
- Code FPA
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dana Point, CA, US
Adverse events under product code FPA
product code FPA- Death
- 95
- Injury
- 14,421
- Malfunction
- 125,815
- Other
- 30
- Total
- 140,361
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.