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

SCOPE LIGHT

K Number: K841825 · Decision Jun 15, 1984
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
76
Review Days
44

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Basic Information

Device Name
SCOPE LIGHT
K Number
K841825
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Zinnanti Surgical Instruments, Inc.
Date Received
May 2, 1984
Decision Date
June 15, 1984
Product Code
HIH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIH Hysteroscope (And Accessories)

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Other Clearances by Zinnanti Surgical Instruments, Inc.

K Number Device Name
K925501 NYLON COATED SPECULA
K941458 UTERINE MANIPULATOR/INJECTOR WITH SPRING
K941457 UTERINE INJECTOR WITH SPRING
K925560 ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES
K925957 SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE
K925960 FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USE
K926021 NEEDLE HOLDERS & ACCESS FOR LAPAR SURG-OB/GYN USE
K925958 SCISSOR FOR LAPAROSCOPIC SURGERY GU USE
K926181 ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY
K926016 NEEDLE HOLDERS & ACCESS FOR LAPAR SURG-GU USE
Search all 76 clearances from Zinnanti Surgical Instruments, Inc. →