FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HEAT MOISTURE CONDENSER

K Number: K923910 · Decision Jan 26, 1993
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
23
Review Days
175

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Basic Information

Device Name
HEAT MOISTURE CONDENSER
K Number
K923910
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Concord/Portex
Date Received
August 4, 1992
Decision Date
January 26, 1993
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

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Other Clearances by Concord/Portex

K Number Device Name
K923559 STERI-CATH MDI
K930218 SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
K924541 EPIDURAL MINIPACK
K930286 DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
K923127 NEEDLE-PRO CARTRIDGE
K922749 LOW PROFILE TRACHEOSTOMY TUBE
K922445 VACU-PRO
K915452 ANESTHESIA BREATHING CIRCUIT
K911809 NEW-VENT
K912124 TRACHEOSTOMY TUBE AND CUFF
Search all 23 clearances from Concord/Portex →