HUMAN C1Q RADIAL IMMUNODIFFUSION KIT— 510(k) K951968
Substantially EquivalentKent Laboratories, Inc.
FDA 510(k) clearance K951968 for HUMAN C1Q RADIAL IMMUNODIFFUSION KIT, Substantially Equivalent on 1995-05-30. Applicant: Kent Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Kent Laboratories, Inc.
- Product code
- Code DAK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5240
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, WA, US
Recent devices under product code DAK
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Data sourced from openFDA. This site is unofficial and independent of the FDA.