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

NA NEEDLES

K Number: K904667 · Decision Dec 12, 1990
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
142
Review Days
58

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Basic Information

Device Name
NA NEEDLES
K Number
K904667
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
October 15, 1990
Decision Date
December 12, 1990
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

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K934835 FLOVAL
K931764 HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES
K915857 FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE
K931994 RESECTOSCOPE SHEATH
K933992 OLYMPUS SCLEROTHERAPY BALLOON
K934361 OLYMPUS CREATININE REAGENT
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