GENIE CUP INTEGRATED SCREENING DEVICE— 510(k) K980836
Substantially EquivalentApplied Technology Ventures, LLC
FDA 510(k) clearance K980836 for GENIE CUP INTEGRATED SCREENING DEVICE, Substantially Equivalent on 1998-06-29. Applicant: Applied Technology Ventures, LLC. Device class: 2.
Clearance details
- Applicant
- Applied Technology Ventures, LLC
- Product code
- Code LDJ
- Device class
- Class 2
- Regulation
- 21 CFR 862.3870
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rockville, MD, US
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More clearances from Applied Technology Ventures, LLC
view allData sourced from openFDA. This site is unofficial and independent of the FDA.