TDX REA LDH— 510(k) K841703
Substantially EquivalentAbbott Laboratories
FDA 510(k) clearance K841703 for TDX REA LDH, Substantially Equivalent on 1984-06-08. Applicant: Abbott Laboratories. Device class: 2.
Clearance details
- Applicant
- Abbott Laboratories
- Product code
- Code CFJ
- Device class
- Class 2
- Regulation
- 21 CFR 862.1440
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Abbott Park, IL, US
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