QUINTEST— 510(k) K953939
Substantially EquivalentBayer Corp.
FDA 510(k) clearance K953939 for QUINTEST, Substantially Equivalent on 1995-11-13. Applicant: Bayer Corp.. Device class: 2.
Clearance details
- Applicant
- Bayer Corp.
- Product code
- Code SCL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Spokane, WA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.