FDA 510(k) Substantially Equivalent 🇺🇸 United States

P1808 MOBILE C-ARM IMAGE INTENSIFIER

K Number: K827087 · Decision Mar 4, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
13
Review Days
41

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Basic Information

Device Name
P1808 MOBILE C-ARM IMAGE INTENSIFIER
K Number
K827087
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Precise Optics
Date Received
January 22, 1982
Decision Date
March 4, 1982
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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