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

TUTTNAUER LSI (AUTOMATIC)

K Number: K920478 · Decision Jul 8, 1993
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
6
Review Days
526

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Basic Information

Device Name
TUTTNAUER LSI (AUTOMATIC)
K Number
K920478
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tuttnauer Co. , Ltd.
Date Received
January 29, 1992
Decision Date
July 8, 1993
Product Code
FLE
Advisory Committee
General Hospital
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
FLE Sterilizer, Steam

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Other Clearances by Tuttnauer Co. , Ltd.

K Number Device Name
K111736 TUTTNAUER EZ PLUS SERIES ELECTRONIC TABLETOP AUTOCLAVES
K063711 TUTTNAUER PREVACUUM STEAM HEATED AUTOCLAVE, MODELS 6990 SP-1A, 66120 SP-1A, 69150 SP-2A, 69120 L USA SP-2A, 69180 SP-2HA
K003470 EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870
K850264 TUTTNAUER PRE-VACUUM AUTOCLAVE
K833837 AMERICAN GOLD SERIES AUTOCLAVE