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

MODIFIED AIRE-CUF SILICONE TRACHEOSTOMY TUBE

K Number: K896548 · Decision Jan 22, 1990
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
50
Review Days
68

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Basic Information

Device Name
MODIFIED AIRE-CUF SILICONE TRACHEOSTOMY TUBE
K Number
K896548
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Bivona Medical Technologies
Date Received
November 15, 1989
Decision Date
January 22, 1990
Product Code
JOH
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
JOH Tube Tracheostomy And Tube Cuff

Similar 510(k) Clearances

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Other Clearances by Bivona Medical Technologies

K Number Device Name
K952700 SUPERSLICK
K942025 BURGET NASAL STENT
K944178 BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES
K935053 BIVONA NASAL TURBINATE STENT
K933398 BIVONA ILLUMINATED ENDOTRACHEAL TUBE
K931749 BIVONA(R) ICU ENDOTRACHEAL TUBE
K922665 BIVONA HYPERFLEX TRACHEOSTOMY TUBE
K923878 BIVONA CUSTOMIZED TRACHEOSTOMY TUBES
K920604 BIVONA TRACHEAL T-TUBE STENT
K915761 BIVONA-COLORADO VOICE PROSTHESIS
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