FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DIENER RETRIEVAL DEVICES

K Number: K950559 · Decision Feb 16, 1995
Classifications
1
FEI Numbers
188
Registration Numbers
188
Same Product Code
38
Applicant Total
46
Review Days
8

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Basic Information

Device Name
DIENER RETRIEVAL DEVICES
K Number
K950559
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mill-Rose Laboratory
Date Received
February 8, 1995
Decision Date
February 16, 1995
Product Code
FCL
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
FCL Forceps, Biopsy, Non-Electric

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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
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 →