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

EC-3870CILK, CONFOCAL VIDEO COLONOSCOPE

K Number: K042741 · Decision Oct 19, 2004
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
12
Review Days
15

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Basic Information

Device Name
EC-3870CILK, CONFOCAL VIDEO COLONOSCOPE
K Number
K042741
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
October 4, 2004
Decision Date
October 19, 2004
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
Y

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

Similar 510(k) Clearances

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

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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
K061068 EG-3670URK
Search all 12 clearances from Pentax Medical Company →