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

MILL-ROSE DISPOSABLE POLYPECTOMY SNARE

K Number: K971275 · Decision May 23, 1997
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
46
Review Days
46

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Basic Information

Device Name
MILL-ROSE DISPOSABLE POLYPECTOMY SNARE
K Number
K971275
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mill-Rose Laboratory
Date Received
April 7, 1997
Decision Date
May 23, 1997
Product Code
FDI
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
FDI Snare, Flexible

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Other Clearances by Mill-Rose Laboratory

K Number Device Name
K983122 MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) COMBINATION CYTOLOGY/HISTOLOGY PROCEDURAL KIT
K983124 MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KIT
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
K946293 MILL-ROSE SCOPE CLEANING BRUSH
Search all 46 clearances from Mill-Rose Laboratory →