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

ANGIOMED FINE NEEDLES AND NEEDLE SET

K Number: K855141 · Decision Jan 24, 1986
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
24
Review Days
29

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Basic Information

Device Name
ANGIOMED FINE NEEDLES AND NEEDLE SET
K Number
K855141
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
December 26, 1985
Decision Date
January 24, 1986
Product Code
GAA
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
GAA Needle, Aspiration And Injection, Disposable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GAA), 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
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
Search all 24 clearances from Angiomed U.S., Inc. →