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

RUSCH BRONCHUS BLOCKER KIT

K Number: K010596 · Decision Nov 21, 2001
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
33
Applicant Total
43
Review Days
266

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Basic Information

Device Name
RUSCH BRONCHUS BLOCKER KIT
K Number
K010596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5740
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
February 28, 2001
Decision Date
November 21, 2001
Product Code
CBI
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
CBI Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)

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Other Clearances by Rusch Intl.

K Number Device Name
K033023 INTERMITTENT URETHRAL CATHETERS
K030559 RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEM
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. →