TYPE 1 & 2 (HUMIDAIR I & II)— 510(k) K953507

Substantially Equivalent

Icor AB

FDA 510(k) clearance K953507 for TYPE 1 & 2 (HUMIDAIR I & II), Substantially Equivalent on 1995-09-07. 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: 1995-07-26
Decision date: 1995-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bromma, SE

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Recent devices under product code BYD

K955008 — HEAT & MOISTURE EXCHANGER1996-01-30
K954194 — DISPOSABLE HME/FILTER1995-10-20
K953580 — HEAT MOISTURE EXCHANGER1995-09-15
K953491 — HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE1995-08-25
K953540 — EEE1995-08-25

More clearances from Icor AB

K954402 — ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)1996-05-22
K952325 — ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)1995-07-31
K952823 — FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE1995-07-13
K941987 — HEAT AND MOISTURE EXCHANGERS AND FILTERS1994-08-15
K940041 — COLIBRI1994-07-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.