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

MEYER FOREIGN BODY LOCATOR

K Number: K920470 · Decision Aug 26, 1992
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
175
Applicant Total
1
Review Days
211

Basic Information

Device Name
MEYER FOREIGN BODY LOCATOR
K Number
K920470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SEYMOUR W. MEYER
Date Received
January 28, 1992
Decision Date
August 26, 1992
Product Code
IZH
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
IZH System, X-Ray, Mammographic

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