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

PATIENT POSITIONING ACCESSORIES

K Number: K895500 · Decision Nov 6, 1989
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
14
Review Days
55

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Basic Information

Device Name
PATIENT POSITIONING ACCESSORIES
K Number
K895500
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Perkins Mfg. Co.
Date Received
September 12, 1989
Decision Date
November 6, 1989
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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K915232 GRUNDIG ELECTRONICS VARIOUS MODELS
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K904986 PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060
K904540 VIDEO SYSTEM INTERFACE MODELS
K896615 CINE CAMERA CONTROL MODEL PK2037
K893644 PK2025/PK2045 PROGRAMMABLE VIDEO CONTROLLER
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