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

TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE

K Number: K851856 · Decision May 23, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
33
Applicant Total
39
Review Days
27

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Basic Information

Device Name
TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE
K Number
K851856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5740
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Sheridan Catheter Corp.
Date Received
April 26, 1985
Decision Date
May 23, 1985
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 Sheridan Catheter Corp.

K Number Device Name
K922894 LAZER-TRACH TRACHEAL TUBE
K897046 LASER RESISTANT TRACHEAL TUBE
K890823 ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER
K884765 CLINICAL ELECTRONIC THERMOMETERS
K882918 KIM NASO-INTESTINAL TUBE
K882127 CLINICAL ELECTRONIC THERMOMETERS
K881368 CLINICAL ELECTONIC THERMOMETERS
K881293 SHERIDAN ELECTROSURGERY PROTECTION FILTER
K881873 INTRODUCTION/DRAINAGE CATHETER & ACCESS
K880960 NDYAG LASER TRACHEAL TUBE
Search all 39 clearances from Sheridan Catheter Corp. →