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

SHEATHES, STERILE SHEATHES

K Number: K925869 · Decision Jan 6, 1994
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
17
Review Days
413

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Basic Information

Device Name
SHEATHES, STERILE SHEATHES
K Number
K925869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mayer Laboratories
Date Received
November 19, 1992
Decision Date
January 6, 1994
Product Code
ITX
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
ITX Transducer, Ultrasonic, Diagnostic

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