FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Cassette Autoclave (ACA5)

K Number: K250164 · Decision Aug 14, 2025
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
3
Review Days
205

Basic Information

Device Name
Cassette Autoclave (ACA5)
K Number
K250164
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guangzhou Ajax Medical Equipment Co., Ltd.
Date Received
January 21, 2025
Decision Date
August 14, 2025
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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