VACUETTE PREMIUM SAFETY NEEDLE SYSTEM— 510(k) K072602
Substantially EquivalentMedpro Safety Products, Inc.
FDA 510(k) clearance K072602 for VACUETTE PREMIUM SAFETY NEEDLE SYSTEM, Substantially Equivalent on 2008-06-18. Applicant: Medpro Safety Products, Inc..
Clearance details
- Applicant
- Medpro Safety Products, Inc.
- Product code
- Code FMI
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Lexington, KY, US
Adverse events under product code FMI
product code FMI- Death
- 28
- Injury
- 1,517
- Malfunction
- 23,981
- Other
- 18
- Total
- 25,544
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.