FDA 510(k) Substantially Equivalent 🇺🇸 United States

HISTOCAN BIOPSY NEEDLE

K Number: K813081 · Decision Dec 29, 1981
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
41
Review Days
57

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Basic Information

Device Name
HISTOCAN BIOPSY NEEDLE
K Number
K813081
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Burron Medical Products, Inc.
Date Received
November 2, 1981
Decision Date
December 29, 1981
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

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