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

PIVOTING COMPENSATING FILTERS FOR THE HEAD

K Number: K972766 · Decision Aug 14, 1997
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
13
Review Days
21

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Basic Information

Device Name
PIVOTING COMPENSATING FILTERS FOR THE HEAD
K Number
K972766
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Octostop, Inc.
Date Received
July 24, 1997
Decision Date
August 14, 1997
Product Code
KPR
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
KPR System, X-Ray, Stationary

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Other Clearances by Octostop, Inc.

K Number Device Name
K963941 THE PHARAOH COMPENSATING FILTER
K953246 OCTOROLL
K952871 RIDGES PLUS
K942916 OCTOPAQUE UNIVERSAL
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. →