FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE

K Number: K955238 · Decision Feb 6, 1996
Classifications
1
FEI Numbers
133
Registration Numbers
133
Same Product Code
31
Applicant Total
43
Review Days
84

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Basic Information

Device Name
RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE
K Number
K955238
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5790
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch Intl.
Date Received
November 14, 1995
Decision Date
February 6, 1996
Product Code
BSR
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
BSR Stylet, Tracheal Tube

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. →