FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODELS 54601/54602/54603/54604 NEEDLE & BIOPSY KIT

K Number: K864329 · Decision Dec 3, 1986
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
56
Review Days
29

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Basic Information

Device Name
MODELS 54601/54602/54603/54604 NEEDLE & BIOPSY KIT
K Number
K864329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Dlp, Inc.
Date Received
November 4, 1986
Decision Date
December 3, 1986
Product Code
KNW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNW Instrument, Biopsy

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K913098 APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501
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