LD-1— 510(k) K900107
Substantially EquivalentBoehringer Mannheim Corp.
FDA 510(k) clearance K900107 for LD-1, Substantially Equivalent on 1990-01-18. Applicant: Boehringer Mannheim Corp.. Device class: 1.
Clearance details
- Applicant
- Boehringer Mannheim Corp.
- Product code
- Code DET
- Device class
- Class 1
- Regulation
- 21 CFR 866.5560
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
More clearances from Boehringer Mannheim Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.