EL-RF TEST SYSTEM: EL-RF-IGM KIT— 510(k) K933712
Substantially EquivalentTheratest Laboratories, Inc.
FDA 510(k) clearance K933712 for EL-RF TEST SYSTEM: EL-RF-IGM KIT, Substantially Equivalent on 1994-01-28. Applicant: Theratest Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Theratest Laboratories, Inc.
- Product code
- Code DHR
- Device class
- Class 2
- Regulation
- 21 CFR 866.5775
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.