FDA 510(k) Substantially Equivalent 🇺🇸 United States

BRONCHOFIBERSCOPE, FB-19A

K Number: K770879 · Decision May 25, 1977
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
39
Review Days
9

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Basic Information

Device Name
BRONCHOFIBERSCOPE, FB-19A
K Number
K770879
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
May 16, 1977
Decision Date
May 25, 1977
Advisory Committee
Unknown
Review Advisory Committee
GU
Third Party
N

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