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

ASPIRATION/INJECTION NEEDLE

K Number: K913992 · Decision Oct 30, 1991
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
55
Review Days
55

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Basic Information

Device Name
ASPIRATION/INJECTION NEEDLE
K Number
K913992
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Northgate Technologies, Inc.
Date Received
September 5, 1991
Decision Date
October 30, 1991
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

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K120151 NEBULAE I
K041560 FLO-ASSISTANT
K033614 MISTIC HUMIDIFICATION SYSTEM 850-00/01/02, 2215
K022052 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0
K010053 HUMI-FLOW, MODEL 6-850-00/ 01/02
K011928 HYDROTOWER ARTHROSCOPIC ADMINISTRATION TUBING SET, MODEL 7-460-05
K001325 FLO ASSISTANT, MODEL 4-250-00
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