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

Saberscope5 Laparoscope

K Number: K220872 · Decision Apr 20, 2022
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
4
Review Days
26

Basic Information

Device Name
Saberscope5 Laparoscope
K Number
K220872
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xenocor, Inc
Date Received
March 25, 2022
Decision Date
April 20, 2022
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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