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

CELERITY HP Indicator Tape (PCC077)

K Number: K242189 · Decision Aug 20, 2024
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
21
Review Days
26

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Basic Information

Device Name
CELERITY HP Indicator Tape (PCC077)
K Number
K242189
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Steris
Date Received
July 25, 2024
Decision Date
August 20, 2024
Product Code
JOJ
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
JOJ Indicator, Physical/Chemical Sterilization Process

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K242773 Electro Lube NXT
DEN230085 VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein (CPP) Indicator
K241344 MetriCide™ OPA Plus Solution Test Strip
K241055 Electro Lube NXT
K240760 CELERITY HP Indicator Tape
K232826 Articulator Injection Needle (00711807), Articulator Injection Needle (00711810), Articulator Injection Needle - enteroscope (00711808), Carr-Locke Injection Needle (00711811), Carr-Locke Injection Needle (00711812), Carr-Locke Injection Needle (00711813), Carr-Locke Injection Needle (00711814), Carr-Locke Injection Needle (00711822), Carr-Locke Injection Needle (00711823), Carr-Locke Injection Needle (00711824)
K233654 VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid Chemical Sterilant Processing Systems
K233187 Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)
Search all 21 clearances from Steris →