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

MODUMED MUGX

K Number: K780368 · Decision Mar 14, 1978
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
16
Applicant Total
468
Review Days
7

Basic Information

Device Name
MODUMED MUGX
K Number
K780368
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1310
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
MEDTRONIC VASCULAR
Date Received
March 7, 1978
Decision Date
March 14, 1978
Product Code
JWM
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
JWM System, Tomographic, Nuclear

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