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

EG-3670URK

K Number: K061068 · Decision May 3, 2006
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
42
Applicant Total
12
Review Days
16

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
EG-3670URK
K Number
K061068
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 Company
Date Received
April 17, 2006
Decision Date
May 3, 2006
Product Code
ODG
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
ODG Endoscopic Ultrasound System, Gastroenterology-Urology

Similar 510(k) Clearances

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

View all

Other Clearances by Pentax Medical Company

K Number Device Name
K131946 ENTAX ULTRASOUND VIDEO BRONCHOSCOPE EB-1970UK + HI VISIN PREIRUS
K131028 PENTAX VIDEO BRONCHOSCOPES (EB FAMILY)
K131902 PENTAX VIDEO UPPER G.I. SCOPES (EG FAMILY)
K131855 PENTAX VIDEO COLONOSCOPES (EC FAMILY)
K093037 PENTEX EC-3890LI
K092710 PENTAX ED-3490TK, VIDEO DUODENOSCOPE
K090197 EG-3870UTK
K090196 EG-3670URK
K081518 ULTRASOUND VIDEO BRONCHOSCOPE, MODEL EB-1970UK
K042741 EC-3870CILK, CONFOCAL VIDEO COLONOSCOPE
Search all 12 clearances from Pentax Medical Company →