FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OLYMPUS LF-1 INTUBATION SCOPE

K Number: K850978 · Decision May 23, 1985
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
7
Applicant Total
142
Review Days
76

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Basic Information

Device Name
OLYMPUS LF-1 INTUBATION SCOPE
K Number
K850978
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5530
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
March 8, 1985
Decision Date
May 23, 1985
Product Code
CAL
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAL Laryngoscope, Non-Rigid

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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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