AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II— 510(k) K042975
Substantially EquivalentAmeditech, Inc.
FDA 510(k) clearance K042975 for AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II, Substantially Equivalent on 2004-12-29. Applicant: Ameditech, Inc.. Device class: 2.
Clearance details
- Applicant
- Ameditech, Inc.
- Product code
- Code DIS
- Device class
- Class 2
- Regulation
- 21 CFR 862.3150
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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