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

WIS1000

K Number: K112621 · Decision May 30, 2012
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
1
Review Days
265

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Basic Information

Device Name
WIS1000
K Number
K112621
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Foreseeson Custom Displays, Inc.
Date Received
September 8, 2011
Decision Date
May 30, 2012
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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