HUMAPEN LUXURA HD— 510(k) K063151
Substantially EquivalentEli Lilly and Co.
FDA 510(k) clearance K063151 for HUMAPEN LUXURA HD, Substantially Equivalent on 2007-01-09. Applicant: Eli Lilly and Co.. Device class: 2.
Clearance details
- Applicant
- Eli Lilly and Co.
- Product code
- Code NSC
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
More clearances from Eli Lilly and Co.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.