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

BIOPSY FORCEPS W/OVAL CUP & NEEDLE

K Number: K820980 · Decision Apr 26, 1982
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
46
Review Days
20

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Basic Information

Device Name
BIOPSY FORCEPS W/OVAL CUP & NEEDLE
K Number
K820980
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Mill-Rose Laboratory
Date Received
April 6, 1982
Decision Date
April 26, 1982
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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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 →