QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC— 510(k) K070098
Substantially EquivalentPhamatech, Inc.
FDA 510(k) clearance K070098 for QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC, Substantially Equivalent on 2007-12-07. Applicant: Phamatech, Inc.. Device class: 2.
Clearance details
- Applicant
- Phamatech, 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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view allData sourced from openFDA. This site is unofficial and independent of the FDA.