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

Sterilization Pouch/Roll

K Number: K251347 · Decision Jan 28, 2026
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
1
Review Days
273

Basic Information

Device Name
Sterilization Pouch/Roll
K Number
K251347
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sterivic Medical Co., Ltd.
Date Received
April 30, 2025
Decision Date
January 28, 2026
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

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