FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
QUARK SERIES
K Number: K120146
·
Decision Dec 11, 2012
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
10
Review Days
328
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Basic Information
- Device Name
- QUARK SERIES
- K Number
- K120146
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5895
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cosmed Srl
- Date Received
- January 18, 2012
- Decision Date
- December 11, 2012
- Product Code
- CBK
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | FDA class 2 | Anesthesiology |
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| K071533 | FITMATE SERIES | Sep 28, 2007 | Substantially Equivalent |
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| K014262 | COSMED QUARK C12/QUARK T12 | Mar 26, 2002 | Substantially Equivalent |
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| K963373 | COSMED K4 | Sep 10, 1997 | Substantially Equivalent |