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

OLYMPUS RIGID URETERORENOSCOPE

K Number: K852888 · Decision Aug 21, 1985
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
142
Review Days
43

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Basic Information

Device Name
OLYMPUS RIGID URETERORENOSCOPE
K Number
K852888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
July 9, 1985
Decision Date
August 21, 1985
Product Code
FGB
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
FGB Ureteroscope And Accessories, Flexible/Rigid

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Other Clearances by Olympus Corp.

K Number Device Name
K915402 EW-10 AND EW-20
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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
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