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

ClearCam System

K Number: K200228 · Decision Feb 19, 2020
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
1
Review Days
20

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Basic Information

Device Name
ClearCam System
K Number
K200228
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clearcam, LLC
Date Received
January 30, 2020
Decision Date
February 19, 2020
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
Y

Classifications

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

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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