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

DANA REUSABLE TEST PACK FOR STEAM STERILIZATION

K Number: K102761 · Decision Dec 20, 2010
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
9
Review Days
88

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DANA REUSABLE TEST PACK FOR STEAM STERILIZATION
K Number
K102761
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dana Products, Inc.
Date Received
September 23, 2010
Decision Date
December 20, 2010
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

Other 510(k) clearances with the same product code (JOJ), ordered by most recent decision date.

View all

Other Clearances by Dana Products, Inc.

K Number Device Name
K133267 DANA REUSABLE TEST PACK
K130135 DANA REUSABLE BI TEST PACK
K120592 DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS
K110253 REUSABLE TEST PACK FOR DANA EMULATING INDICATORS
K103321 DANA REUSABLE TESTPACK FOR STEAM STERILIZATION FOR 10 MINUTE EXTENDED CYCLES
K100891 DANA EMULATING INDICATOR
K092944 DANA REUSABLE TEST PACK FOR STEAM STERILIZATION
K012195 STEAM STERILIZATION INTERGRATOR