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

TEC 2720 MAMEX DC MAG

K Number: K854203 · Decision Mar 6, 1986
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
18
Review Days
141

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
TEC 2720 MAMEX DC MAG
K Number
K854203
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Tecnomed, Inc.
Date Received
October 16, 1985
Decision Date
March 6, 1986
Product Code
IZH
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
IZH System, X-Ray, Mammographic

Similar 510(k) Clearances

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

View all

Other Clearances by Tecnomed, Inc.

K Number Device Name
K892226 TEC 6340 90/15 RADIOGRAPHIC/FLUOROSCOPIC TABLE
K827124 RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHIC
K820306 RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC
K820307 TECNOMED GENERATOR, RADIOGRAPH., 3 PHASE
K827126 TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE
K827125 RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC
K820305 RALCO COLLIMATORS, MANUAL RADIOGRAPHIC
K811197 SUPERIX 120
K811195 ARGOSTAT
K811196 ALLMEC 90/15
Search all 18 clearances from Tecnomed, Inc. →