MULTICHEM P
FDA 510(k) clearance K131992 · decided 2013-09-25
Clearance details
- K-number
- K131992
- Device name
- MULTICHEM P
- Applicant
- Techno-Path Manufacturing , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2013-06-28
- Decision date
- 2013-09-25
- Days to decision
- 89 days
- Clearance type
- Abbreviated
- Product code
- JJY
- Device class
- 1
- Regulation number
- 862.1660
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Highland Village, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.