ICOR AGENT MONITOR— 510(k) K883532
Substantially EquivalentIcor AB
FDA 510(k) clearance K883532 for ICOR AGENT MONITOR, Substantially Equivalent on 1988-11-04. Applicant: Icor AB. Device class: 2.
Clearance details
- Applicant
- Icor AB
- Product code
- Code CBQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.1500
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bromma, SE
Recent devices under product code CBQ
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- K952325 — ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
- K952823 — FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE
- K941987 — HEAT AND MOISTURE EXCHANGERS AND FILTERS
Data sourced from openFDA. This site is unofficial and independent of the FDA.