FDA 510(k) FDA class 1 Substantially Equivalent 🇸🇪 Sweden

TYPE 1 & 2 (HUMIDAIR I & II)

K Number: K953507 · Decision Sep 7, 1995
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
16
Review Days
43

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Basic Information

Device Name
TYPE 1 & 2 (HUMIDAIR I & II)
K Number
K953507
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Icor AB
Date Received
July 26, 1995
Decision Date
September 7, 1995
Product Code
BYD
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
BYD Condenser, Heat And Moisture (Artificial Nose)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BYD), ordered by most recent decision date.

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Other Clearances by Icor AB

K Number Device Name
K954402 ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
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
K940041 COLIBRI
K941436 AFH, AFH FLEX, AFH/T, AFH/T FLEX, AF
K925622 FHB, FHB-T, FHBFLEX, FHBFLEX-T
K914416 BREATH-EASY, MODIFICATION
K904338 ICOR HCH 4, ICOR HCH 7
K900150 HCH 9165, 9165 S, 9166, HFH, HFH-T HEAT MOISTURE
Search all 16 clearances from Icor AB →