AIA-PACK CPR ASSAY— 510(k) K951848
Substantially EquivalentTosoh Medics, Inc.
FDA 510(k) clearance K951848 for AIA-PACK CPR ASSAY, Substantially Equivalent on 1996-02-13. Applicant: Tosoh Medics, Inc.. Device class: 1.
Clearance details
- Applicant
- Tosoh Medics, Inc.
- Product code
- Code JKD
- Device class
- Class 1
- Regulation
- 21 CFR 862.1135
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foster City, CA, US
Recent devices under product code JKD
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