ICOR CMU Q PLUS— 510(k) K895935
Substantially EquivalentIcor AB
FDA 510(k) clearance K895935 for ICOR CMU Q PLUS, Substantially Equivalent on 1990-01-04. Applicant: Icor AB. Device class: 2.
Clearance details
- Applicant
- Icor AB
- Product code
- Code BZL
- Device class
- Class 2
- Regulation
- 21 CFR 868.1730
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bromma, SE
Recent devices under product code BZL
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- K941987 — HEAT AND MOISTURE EXCHANGERS AND FILTERS
Data sourced from openFDA. This site is unofficial and independent of the FDA.