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

RUSCH REINFORCED ENDOTRACHEAL (OR TRACHEAL) TUBE- CUFFED AND UNCUFFED MURPHY/MAGILL, STERILE

K Number: K990619 · Decision Aug 3, 1999
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
43
Review Days
159

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Basic Information

Device Name
RUSCH REINFORCED ENDOTRACHEAL (OR TRACHEAL) TUBE- CUFFED AND UNCUFFED MURPHY/MAGILL, STERILE
K Number
K990619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
February 25, 1999
Decision Date
August 3, 1999
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

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Other Clearances by Rusch Intl.

K Number Device Name
K033023 INTERMITTENT URETHRAL CATHETERS
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K023666 RUSCH GUIDED CHOLANGIOGRAPHY CATHETER
K023918 RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESS
K023964 RUSCH MICROLARYNGEAL TUBE
K021540 RUSCH EDGAR TUBE
K021764 RUSCH TRACHEOFIX SET, CUFFED AND UNCUFFED
K020714 RUSCH FLONEIL; FLOCATH INTROGEL
K010798 RUSCH CANTOR TUBE
K010797 RUSCH MILLER-ABBOTT TUBE
Search all 43 clearances from Rusch Intl. →