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

BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO

K Number: K801950 · Decision Oct 3, 1980
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
25
Applicant Total
8
Review Days
49

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Basic Information

Device Name
BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO
K Number
K801950
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1860
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
B C Medical , Ltd.
Date Received
August 15, 1980
Decision Date
October 3, 1980
Product Code
KPX
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
KPX Changer, Radiographic Film/Cassette

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K870205 ROTAX-II BI-PLANE CIRCULAR ARM
K801949 BCM-302 COLLIMATING CONE & COMPENSATIN