DRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL— 510(k) K913650
Substantially EquivalentDuo Research, Inc.
FDA 510(k) clearance K913650 for DRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL, Substantially Equivalent on 1991-09-06. Applicant: Duo Research, Inc.. Device class: 1.
Clearance details
- Applicant
- Duo Research, Inc.
- Product code
- Code DIF
- Device class
- Class 1
- Regulation
- 21 CFR 862.3280
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Annapolis, MD, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.