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

ARGYLE ESOPHAGEAL STETHOSCOPE

K Number: K790523 · Decision Mar 27, 1979
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
12
Applicant Total
62
Review Days
12

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Basic Information

Device Name
ARGYLE ESOPHAGEAL STETHOSCOPE
K Number
K790523
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1910
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Industries
Date Received
March 15, 1979
Decision Date
March 27, 1979
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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K792014 LANCER L-INA BUFFER, POLYMER, WASH SOLU
K782077 LANCER ICE CUBE
K790196 MONOJECT ARTERIAL BLOOD SAMPLING DEVICE
K790197 REAGENT KIT, LANCER GLUCOSE
K781459 MONOJECT SCALE MAGNIFIER
K781060 MONOJECT ENDOSSEOUS DENTAL IMPLANT
K772149 LANCER BIOPSY HOLDER
Search all 62 clearances from Sherwood Medical Industries →