FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇷 Türkiye

PMSSteripack Self-Seal Sterilization Pouch with Chemical Indicator (KP)

K Number: K152669 · Decision Jan 15, 2016
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
1
Review Days
120

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Basic Information

Device Name
PMSSteripack Self-Seal Sterilization Pouch with Chemical Indicator (KP)
K Number
K152669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pms Tip Teknolojileri Sanayi VE Ticaret Limited Std
Date Received
September 17, 2015
Decision Date
January 15, 2016
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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