FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Nam illumination probe with chopper

K Number: K202670 · Decision Aug 20, 2021
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
39
Applicant Total
1
Review Days
340

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Nam illumination probe with chopper
K Number
K202670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oculight , Ltd.
Date Received
September 14, 2020
Decision Date
August 20, 2021
Product Code
MPA
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
MPA Endoilluminator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MPA), ordered by most recent decision date.

View all