3M Attest Steam Chemical Integrators
K-Number: K191236 · 2019-11-22
Applicant3M Company
Decision Date2019-11-22
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
3M Attest Steam Chemical Integrators is a medical device manufactured by 3M Company. It received FDA 510(k) clearance on 2019-11-22 under approval number K191236. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 3M Attest Steam Chemical Integrators?
3M Attest Steam Chemical Integrators is a medical device that received FDA 510(k) clearance on 2019-11-22. It is manufactured by 3M Company. The 510(k) number is K191236.
When was 3M Attest Steam Chemical Integrators approved by the FDA?
3M Attest Steam Chemical Integrators received FDA 510(k) clearance on 2019-11-22, under approval number K191236.
What company makes 3M Attest Steam Chemical Integrators?
3M Attest Steam Chemical Integrators is manufactured by 3M Company.
What is the FDA product code for 3M Attest Steam Chemical Integrators?
The FDA product code for 3M Attest Steam Chemical Integrators is JOJ.
Other Devices by 3M Company
K163207Filtek One Bulk Fill Restorative
K1605463M Attest Rapid Readout Biological Indicator
K1713733M Bair Hugger Model 675 Total Temperature Management System
K1703213M Comply Hydrogen Peroxide Chemical Indicator 1248
K1705633M Comply Hydrogen Peroxide Indicator Tape
K1710033M Attest Rapid Readout Biological Indicator, 3M Attest Auto-reader
Related Devices (Code: JOJ)
K161024Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization TapeCanadian Technical Tape, Ltd.
K160485VERIFY VH2O2 Indicator TapeSTERIS Corporation
K152630VERIFY STEAM Integrating IndicatorSTERIS Corporation
K152394Rapicide PA High-Level Disinfectant Test StripsMedivators, Inc.
K172472Micro-MEC 1.8% Glutaraldehyde Monitor StripSTERIS Corporation
K170439AN87 DosimeterAndersen Sterilizers, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.