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

SHERIDAN/ESOPHAGEAL STETHOSCOPE

K Number: K830218 · Decision Mar 9, 1983
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
12
Applicant Total
39
Review Days
44

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Basic Information

Device Name
SHERIDAN/ESOPHAGEAL STETHOSCOPE
K Number
K830218
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1910
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Sheridan Catheter Corp.
Date Received
January 24, 1983
Decision Date
March 9, 1983
Product Code
BZW
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
BZW Stethoscope, Esophageal

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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. →