FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT

K Number: K935858 · Decision Feb 22, 1994
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
46
Review Days
76

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Basic Information

Device Name
MILL-ROSE PERCUTANEOUS PROCEDURAL KIT
K Number
K935858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Mill-Rose Laboratory
Date Received
December 8, 1993
Decision Date
February 22, 1994
Product Code
LRO
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
LRO General Surgery Tray

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K Number Device Name
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K983124 MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KIT
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
Search all 46 clearances from Mill-Rose Laboratory →