FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

STATIM 5000 CASSETTE AUTOCLAVE

K Number: K983679 · Decision Jan 4, 1999
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
9
Review Days
76

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
STATIM 5000 CASSETTE AUTOCLAVE
K Number
K983679
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Scican
Date Received
October 20, 1998
Decision Date
January 4, 1999
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLE), ordered by most recent decision date.

View all

Other Clearances by Scican

K Number Device Name
K062418 K-SPRAY, MODEL 085-2715
K021064 QUANTIM 16 AUTOCLAVE
K964691 TCB TEMPORARY CROWN AND BRIDGE MATERIAL
K962179 STAT IM 5000 CASSETTE AUTOCLAVE
K944036 STERIMASTER AUTOCLAVE
K945142 POLYSIL (VINYL POLYSILOXAN IMPRESSION MATERIAL)
K915054 STATIM CASSETT AUTOCLAVE, MODIFICATION
K910241 STATIM CASSETTE AUTOCLAVE