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

TRANSESOPHAGEAL ECHO TRANSDUCER

K Number: K883889 · Decision Nov 29, 1988
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
254
Review Days
76

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Basic Information

Device Name
TRANSESOPHAGEAL ECHO TRANSDUCER
K Number
K883889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
General Electric Co.
Date Received
September 14, 1988
Decision Date
November 29, 1988
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOP Transducer, Ultrasonic

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