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

ACCESS TM

K Number: K894290 · Decision Sep 7, 1989
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
42
Review Days
76

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Basic Information

Device Name
ACCESS TM
K Number
K894290
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Diasonics, Inc.
Date Received
June 23, 1989
Decision Date
September 7, 1989
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

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Other Clearances by Diasonics, Inc.

K Number Device Name
K962662 VINGMED SOUND COLOR FLOW MAPPING SYSTEM
K924079 CFM-800 COLOR FLOW MAPPING SYSTEM
K911435 CPA/3.5 MHZ PROBE
K905200 SACA, 3.5 MHZ PROBE
K903562 CW DOPPLER 2.25 MHZ PROBE
K903984 CW DOPPLER/4.5 MHZ
K896637 ACCESS(TM), SOFTWARE RELEASE 4.11P
K893518 MT/S SOFTWARE RELEASE 5.0.
K893881 ACCESS TM
K891452 SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE
Search all 42 clearances from Diasonics, Inc. →