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

FLOVAL

K Number: K934835 · Decision Jun 21, 1994
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
23
Applicant Total
142
Review Days
256

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Basic Information

Device Name
FLOVAL
K Number
K934835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus Corp.
Date Received
October 8, 1993
Decision Date
June 21, 1994
Product Code
FJL
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
FJL Resectoscope

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K931763 HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS
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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