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

EW-10 AND EW-20

K Number: K915402 · Decision Jun 23, 1995
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
56
Applicant Total
142
Review Days
1297

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Basic Information

Device Name
EW-10 AND EW-20
K Number
K915402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent for Some Indications
Applicant
Olympus Corp.
Date Received
December 4, 1991
Decision Date
June 23, 1995
Product Code
FEB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FEB Accessories, Cleaning, For Endoscope

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K Number Device Name
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K942338 OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES
K931763 HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS
K934835 FLOVAL
K931764 HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES
K915857 FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE
K931994 RESECTOSCOPE SHEATH
K933992 OLYMPUS SCLEROTHERAPY BALLOON
K934361 OLYMPUS CREATININE REAGENT
K934136 OLYMPUS CHLORIDE REAGENT, MODIFICATION
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