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

RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC

K Number: K820306 · Decision Mar 5, 1982
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
15
Applicant Total
18
Review Days
29

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
RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC
K Number
K820306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1610
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Tecnomed, Inc.
Date Received
February 4, 1982
Decision Date
March 5, 1982
Product Code
KPW
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
KPW Device, Beam Limiting, X-Ray, Diagnostic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPW), 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
K854203 TEC 2720 MAMEX DC MAG
K827124 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. →