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

OLYMPUS LUS ULTRASONIC LITHOTRIPTER

K Number: K873367 · Decision Nov 30, 1987
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
13
Applicant Total
142
Review Days
101

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Basic Information

Device Name
OLYMPUS LUS ULTRASONIC LITHOTRIPTER
K Number
K873367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4480
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
August 21, 1987
Decision Date
November 30, 1987
Product Code
FEO
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
FEO Lithotriptor, Ultrasonic

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Other Clearances by Olympus Corp.

K Number Device Name
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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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