FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MOLYBDENUM/RHODIUM FILTERS

K Number: K934686 · Decision May 26, 1994
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
27
Review Days
239

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Basic Information

Device Name
MOLYBDENUM/RHODIUM FILTERS
K Number
K934686
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Continental X-Ray Corp.
Date Received
September 29, 1993
Decision Date
May 26, 1994
Product Code
IZO
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
IZO Generator, High-Voltage, X-Ray, Diagnostic

Similar 510(k) Clearances

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

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Other Clearances by Continental X-Ray Corp.

K Number Device Name
K972442 CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002
K962140 ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300
K961690 CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
K954581 ARC SERIES
K950571 LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270
K942175 LINEAR TOMOGRAPHIC SYSTEM: PMT 6000
K942100 MODEL TM EP HIGH VOLTAGE GENERATOR
K931724 ELECTROPHYSIOLOGY (EP) TABLE EP 2000 SERIES
K925934 WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT
K921986 PATIENT INFORMATION MANAGER (PIM)
Search all 27 clearances from Continental X-Ray Corp. →