FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE— 510(k) K952823
Substantially EquivalentIcor AB
FDA 510(k) clearance K952823 for FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE, Substantially Equivalent on 1995-07-13. Applicant: Icor AB. Device class: 1.
Clearance details
- Applicant
- Icor AB
- Product code
- Code BYD
- Device class
- Class 1
- Regulation
- 21 CFR 868.5375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bromma, SE
Recent devices under product code BYD
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