FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

VARIANT OF OCTOSTOP AND OCTOPAQUE

K Number: K930124 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
8
Applicant Total
13
Review Days
393

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Basic Information

Device Name
VARIANT OF OCTOSTOP AND OCTOPAQUE
K Number
K930124
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1830
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Octostop, Inc.
Date Received
January 12, 1993
Decision Date
February 9, 1994
Product Code
KXH
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
KXH Cradle, Patient, Radiologic

Similar 510(k) Clearances

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

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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
K942916 OCTOPAQUE UNIVERSAL
K940306 OCTOSTOP COMPENSATING FILTERS
K935444 OCTOSTOP(R) CHAIR (NEW MODEL
K930357 ACCESSORY TO UNIVERSAL OCTOPAQUE
K926069 WRIST TRACTION
K913659 LITTLE PRISM
Search all 13 clearances from Octostop, Inc. →