FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

OCTOPAQUE UNIVERSAL

K Number: K942916 · Decision Sep 8, 1994
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
26
Applicant Total
13
Review Days
79

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
OCTOPAQUE UNIVERSAL
K Number
K942916
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Octostop, Inc.
Date Received
June 21, 1994
Decision Date
September 8, 1994
Product Code
IXQ
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
IXQ Table, Radiographic, Stationary Top

Similar 510(k) Clearances

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

View all

Other Clearances by Octostop, Inc.

K Number Device Name
K972766 PIVOTING COMPENSATING FILTERS FOR THE HEAD
K963941 THE PHARAOH COMPENSATING FILTER
K953246 OCTOROLL
K952871 RIDGES PLUS
K940306 OCTOSTOP COMPENSATING FILTERS
K935444 OCTOSTOP(R) CHAIR (NEW MODEL
K930124 VARIANT OF OCTOSTOP AND OCTOPAQUE
K930357 ACCESSORY TO UNIVERSAL OCTOPAQUE
K926069 WRIST TRACTION
K913659 LITTLE PRISM
Search all 13 clearances from Octostop, Inc. →