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

BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES

K Number: K944178 · Decision Oct 27, 1994
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
50
Review Days
62

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Basic Information

Device Name
BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES
K Number
K944178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bivona Medical Technologies
Date Received
August 26, 1994
Decision Date
October 27, 1994
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

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K Number Device Name
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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
K915799 BIVONA SLEEP APNEA TUBE
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