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

EPIDURAL CATHETER MODELS 1210/1200

K Number: K983125 · Decision Nov 17, 1998
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
43
Review Days
70

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Basic Information

Device Name
EPIDURAL CATHETER MODELS 1210/1200
K Number
K983125
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
September 8, 1998
Decision Date
November 17, 1998
Product Code
CAZ
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
CAZ Anesthesia Conduction Kit

Similar 510(k) Clearances

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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. →