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

ANGIOMED VAC-U-CUT BIOPSY NEEDLE

K Number: K862805 · Decision Sep 29, 1986
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
24
Review Days
69

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Basic Information

Device Name
ANGIOMED VAC-U-CUT BIOPSY NEEDLE
K Number
K862805
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
July 22, 1986
Decision Date
September 29, 1986
Product Code
GDM
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
GDM Needle, Aspiration And Injection, Reusable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GDM), ordered by most recent decision date.

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Other Clearances by Angiomed U.S., Inc.

K Number Device Name
K874771 ANGIOMED INTRODUCING SETS
K874585 ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
K864225 ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
K863386 VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS
K863446 ANGIOMED HIGH PRESSURE CONNECTORS
K854910 ANGIOFLOW
K854912 ANGIOMED GUIED WIRES
K854908 UROFLEX
K855142 ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY
K855076 ANGIOMED URETER DIATION SETS
Search all 24 clearances from Angiomed U.S., Inc. →