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

WANG/MILL-ROSE PLEURAL BIOPSY NEEDLE

K Number: K942630 · Decision Jul 12, 1994
Classifications
1
FEI Numbers
198
Registration Numbers
198
Same Product Code
353
Applicant Total
46
Review Days
39

Basic Information

Device Name
WANG/MILL-ROSE PLEURAL BIOPSY NEEDLE
K Number
K942630
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MILL-ROSE LABORATORY
Date Received
June 3, 1994
Decision Date
July 12, 1994
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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K Number Device Name
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K971275 MILL-ROSE DISPOSABLE POLYPECTOMY SNARE
K962736 MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE
K960880 MILL-ROSE BLIND MICROBIOLOGY BRUSH
K954519 WANG TRANSENDOSCOPIC ASPIRATION NEEDLE
K951600 MILL-ROSE ROTATABLE POLYPECTOMY SNARE
K954745 MILL-ROSE RIGID SCOPE CLEANING BRUSHES
K951051 RITE-BITE BIOPSY FORCEPS
K951048 RITE-BITE BIOPSY FORCEPS
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