FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STERI-CATH MDI

K Number: K923559 · Decision Oct 25, 1993
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
23
Review Days
465

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Basic Information

Device Name
STERI-CATH MDI
K Number
K923559
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Concord/Portex
Date Received
July 17, 1992
Decision Date
October 25, 1993
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

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Other Clearances by Concord/Portex

K Number Device Name
K930218 SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
K924541 EPIDURAL MINIPACK
K930286 DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
K923127 NEEDLE-PRO CARTRIDGE
K923910 HEAT MOISTURE CONDENSER
K922749 LOW PROFILE TRACHEOSTOMY TUBE
K922445 VACU-PRO
K915452 ANESTHESIA BREATHING CIRCUIT
K911809 NEW-VENT
K912124 TRACHEOSTOMY TUBE AND CUFF
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