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

M. 1336S CATHODE-RAY TUBE DISPLAY

K Number: K780782 · Decision Jun 14, 1978
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
77
Applicant Total
230
Review Days
33

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Basic Information

Device Name
M. 1336S CATHODE-RAY TUBE DISPLAY
K Number
K780782
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Hewlett-Packard Co.
Date Received
May 12, 1978
Decision Date
June 14, 1978
Product Code
DXJ
Advisory Committee
Cardiovascular
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
DXJ Display, Cathode-Ray Tube, Medical

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