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

STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234

K Number: K001649 · Decision Jun 23, 2000
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
12
Review Days
24

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Basic Information

Device Name
STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234
K Number
K001649
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Steritec Products, Inc.
Date Received
May 30, 2000
Decision Date
June 23, 2000
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

Similar 510(k) Clearances

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Other Clearances by Steritec Products, Inc.

K Number Device Name
K083650 EMU-GRAPH 4 EMULATOR, MODEL CI 144
K080136 INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105
K052516 STERITEC CONTAINER CORD - CI 135, STERITEC PROCESS INDICATOR LABELS - CI 140, STERITEC PROCESS INDICATOR DOTS - CI 137
K040901 STERITEC EMU-GRAPH, MODEL NO. CI 131/US
K024293 BOWIE-DICK MINI PAK, MODEL BD 115
K012732 INTEGRAPH FLASH, MODEL CI 110
K010534 CROSS-CHECKS DUAL, MODEL CI 125
K003533 CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L
K003002 STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123
K002861 EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124
Search all 12 clearances from Steritec Products, Inc. →