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

CORE BIOPSY NEEDLE, CATALOG CODE #54006

K Number: K891537 · Decision Apr 18, 1989
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
56
Review Days
32

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Basic Information

Device Name
CORE BIOPSY NEEDLE, CATALOG CODE #54006
K Number
K891537
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dlp, Inc.
Date Received
March 17, 1989
Decision Date
April 18, 1989
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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K950754 MACRO SUCTION TUBE MODEL NO 10061
K934215 CONTAIN-OR
K915268 CATHETER TWO STAGE VENOUS RETURN
K913077 LANCASTER COOLING JACKET, CAT. CODE #13500/13501
K914608 BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120
K913098 APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501
K912229 IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
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