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

MODIFIED ALPHA MC-9R C-ARM

K Number: K900967 · Decision May 9, 1990
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
81
Applicant Total
24
Review Days
68

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Basic Information

Device Name
MODIFIED ALPHA MC-9R C-ARM
K Number
K900967
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Instrumentarium Imaging, Inc.
Date Received
March 2, 1990
Decision Date
May 9, 1990
Product Code
OXO
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
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

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Other Clearances by Instrumentarium Imaging, Inc.

K Number Device Name
K002472 DELTA 32 AND DELTA 32 TACT
K001928 SIGMA
K000976 DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)
K001171 DELTA 16 TACT
K973642 ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100
K955411 DELTA 16
K925987 INSTRUMENTARIUM MEGA4 HT
K924921 INSTRUMENTARIUM MEGA4 HT
K923581 INSTRUMENTARIUM MEGA4 HT
K924472 INSTRUMENTARIUM MEGA4 HT
Search all 24 clearances from Instrumentarium Imaging, Inc. →