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

CROSS-CHECKS

K Number: K951113 · Decision Aug 19, 1996
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
22
Review Days
528

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Basic Information

Device Name
CROSS-CHECKS
K Number
K951113
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Steritec Products Mfg Co, Inc.
Date Received
March 10, 1995
Decision Date
August 19, 1996
Product Code
LRT
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
LRT Indicator, Sterilization

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K122945 STERITEC GREEN CARD PACK BOWIE-DICK TEST MODEL BD 126
K122555 STERITEC LEAD FREE STERILIZATION PROCESS INDICATOR TAPE
K111150 STERITEC SMART-READ BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR
K103000 SMART READ BIOLOGICAL TEST PACK
K072408 EMU-GRAPH EMULATOR, MODEL CI 131
K000502 STEAM/EO RECORD CARD, MODEL CI 121
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