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

RENAL BIOPSY TRAY

K Number: K850438 · Decision Feb 26, 1985
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
13
Review Days
21

Basic Information

Device Name
RENAL BIOPSY TRAY
K Number
K850438
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Packaging Technologies, Inc.
Date Received
February 5, 1985
Decision Date
February 26, 1985
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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K844611 SINGLE BASIN SET
K844614 IV START KIT
K844612 ACUTE HEMODIALYSIS TRAYS
K834074 PERCUTANEOUS SHEATH INTRODUCER TRAY
K834073 CENTRAL VEIN CATHERIZATION TRAY CC-20
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