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

PROCESS 100 ST

K Number: K833846 · Decision Dec 16, 1983
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
20
Review Days
92

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PROCESS 100 ST
K Number
K833846
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Cgr Medical Corp.
Date Received
September 15, 1983
Decision Date
December 16, 1983
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.

View all

Other Clearances by Cgr Medical Corp.

K Number Device Name
K843926 PRESTILIX 1690
K843235 STENOSCOP
K843985 SUSPENSION 7
K841649 MAXIMAX - 4
K833223 SONEL 3000A
K834306 PHASIX-HIGH FREQUENCY GENERATOR
K833941 ORION
K837412 SATURNE I LINEAR ACCELERATOR
K837465 ALCYON ROTATIONAL COBALT THERAPY
K837336 VERASUN RADIATION THERAPY SIMULATION SYSTEM
Search all 20 clearances from Cgr Medical Corp. →