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

MANUAL BONE MARROW BIOPSY DEVICE

K Number: K993435 · Decision Dec 6, 1999
Classifications
1
FEI Numbers
198
Registration Numbers
198
Same Product Code
353
Applicant Total
18
Review Days
55

Basic Information

Device Name
MANUAL BONE MARROW BIOPSY DEVICE
K Number
K993435
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PROMEX, INC.
Date Received
October 12, 1999
Decision Date
December 6, 1999
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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