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

THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY

K Number: K011210 · Decision Aug 15, 2001
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
43
Review Days
118

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Basic Information

Device Name
THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY
K Number
K011210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
April 19, 2001
Decision Date
August 15, 2001
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

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

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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. →