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

TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE

K Number: K990761 · Decision Jul 9, 1999
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
9
Review Days
123

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Basic Information

Device Name
TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE
K Number
K990761
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tuttnauer U.S.A Co, Ltd.
Date Received
March 8, 1999
Decision Date
July 9, 1999
Product Code
FRG
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
FRG Wrap, Sterilization

Similar 510(k) Clearances

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Other Clearances by Tuttnauer U.S.A Co, Ltd.

K Number Device Name
K232658 T-Top 10 & T-Top T-Top 11
K143311 Pre-vacuum Tabletop Autoclave
K090783 TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE
K032192 PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS 4472 EP-1V AND 5596 EP-1V
K021504 TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
K993856 TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP
K962282 TUTTNAUER PREVACUUM TABLE AUTOCLAVE
K973550 TUTTNAUER TABLE-TOP AUTOCLAVE