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

ARACHNOPHLEBECTOMY NEEDLE

K Number: K000932 · Decision May 17, 2000
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
6
Applicant Total
14
Review Days
55

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Basic Information

Device Name
ARACHNOPHLEBECTOMY NEEDLE
K Number
K000932
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Medical Products, Inc.
Date Received
March 23, 2000
Decision Date
May 17, 2000
Product Code
GAH
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
GAH Stylet, Surgical, General & Plastic Surgery

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