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

ULTRASOUND VIDEO BRONCHOSCOPE, MODEL EB-1970UK

K Number: K081518 · Decision Sep 5, 2008
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
12
Review Days
98

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Basic Information

Device Name
ULTRASOUND VIDEO BRONCHOSCOPE, MODEL EB-1970UK
K Number
K081518
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pentax Medical Company
Date Received
May 30, 2008
Decision Date
September 5, 2008
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EOQ), 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
K061068 EG-3670URK
K042741 EC-3870CILK, CONFOCAL VIDEO COLONOSCOPE
Search all 12 clearances from Pentax Medical Company →