REP HDL ELECTROPHORESIS METHOD— 510(k) K882368
Substantially EquivalentHelena Laboratories
FDA 510(k) clearance K882368 for REP HDL ELECTROPHORESIS METHOD, Substantially Equivalent on 1988-08-08. Applicant: Helena Laboratories.
Clearance details
- Applicant
- Helena Laboratories
- Product code
- Code LBT
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beaumont, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.