FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE

K Number: K874585 · Decision Dec 2, 1987
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
10
Applicant Total
24
Review Days
23

Basic Information

Device Name
ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
K Number
K874585
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Angiomed U.S., Inc.
Date Received
November 9, 1987
Decision Date
December 2, 1987
Product Code
DWO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWO Needle, Biopsy, Cardiovascular

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K862805 ANGIOMED VAC-U-CUT BIOPSY NEEDLE
K863446 ANGIOMED HIGH PRESSURE CONNECTORS
K854910 ANGIOFLOW
K854912 ANGIOMED GUIED WIRES
K854908 UROFLEX
K855142 ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY
K855076 ANGIOMED URETER DIATION SETS
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