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

DYNACAD V1.0

K Number: K041286 · Decision Jul 21, 2004
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
71
Review Days
69

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Basic Information

Device Name
DYNACAD V1.0
K Number
K041286
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mri Devices Corp.
Date Received
May 13, 2004
Decision Date
July 21, 2004
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LNH), ordered by most recent decision date.

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Other Clearances by Mri Devices Corp.

K Number Device Name
K041481 MODEL BBC-127 BIOPSY BREAST COIL
K040349 MODIFICATION TO HRW-127 WRIST ARRAY COIL
K040348 MODIFICATION TO HNC-127-INT NEUROVASCULAR ARRAY COIL
K040288 QSC-127-INT SHOULDER ARRAY COIL SET
K033447 CLIPLOC SOFT TISSUE MARKER 18G/100MM (4), /130MM (5 1/8), /150MM (6), MODELS 12370, 12372, 12376
K033567 MODELS HRK-63-8 PMS AND HRK-127-8 KNEE ARRAY COILS
K032576 BIOPSY BREAST COIL, MODEL BBC
K033151 KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL
K033152 HAC-12 AND HAC-30 HEAD ARRAY COIL
K032633 HRK-63-8 KNEE ARRAY COIL
Search all 71 clearances from Mri Devices Corp. →