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

LOW PROFILE TRACHEOSTOMY TUBE

K Number: K922749 · Decision Sep 2, 1992
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
23
Review Days
86

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Basic Information

Device Name
LOW PROFILE TRACHEOSTOMY TUBE
K Number
K922749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Concord/Portex
Date Received
June 8, 1992
Decision Date
September 2, 1992
Product Code
BTO
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
BTO Tube, Tracheostomy (W/Wo Connector)

Similar 510(k) Clearances

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

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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
K923910 HEAT MOISTURE CONDENSER
K922445 VACU-PRO
K915452 ANESTHESIA BREATHING CIRCUIT
K911809 NEW-VENT
K912124 TRACHEOSTOMY TUBE AND CUFF
Search all 23 clearances from Concord/Portex →