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

PENTAX Medical Video Colonoscope EC34-i10T Series

K Number: K180285 · Decision Oct 26, 2018
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
111
Applicant Total
2
Review Days
267

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
PENTAX Medical Video Colonoscope EC34-i10T Series
K Number
K180285
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pentax Medical of America, Inc.
Date Received
February 1, 2018
Decision Date
October 26, 2018
Product Code
FDF
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FDF Colonoscope And Accessories, Flexible/Rigid

Similar 510(k) Clearances

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

View all

Other Clearances by Pentax Medical of America, Inc.

K Number Device Name
K180292 PENTAX Video Upper G.I. Scope EG34-i10