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

ACCUGUIDE MUSCLE INJECTION MONITOR

K Number: K990793 · Decision Oct 22, 1999
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
52
Applicant Total
9
Review Days
226

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Basic Information

Device Name
ACCUGUIDE MUSCLE INJECTION MONITOR
K Number
K990793
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1350
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Xomed
Date Received
March 10, 1999
Decision Date
October 22, 1999
Product Code
GXZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXZ Electrode, Needle

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K031510 NIM-SPINE
K002972 MEROGEL CONTROL GEL ENT SURGICAL DRESSING
K002224 XPS 3000 SYSTEM
K000728 MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE
K963727 HOFFMAN H/A COATED LONG-TERM VENTILATION TUBE WITH LINER
K963246 TREBAY MICRODEBRIDER OR XPS STRAIGHT SHOT