ACCUTEX CRP LATEX TEST— 510(k) K924332
Substantially EquivalentJ.S. Medical Assoc.
FDA 510(k) clearance K924332 for ACCUTEX CRP LATEX TEST, Substantially Equivalent on 1992-12-07. Applicant: J.S. Medical Assoc.. Device class: 2.
Clearance details
- Applicant
- J.S. Medical Assoc.
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Natick, MA, US
Recent devices under product code DCK
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