LF Process Indicator Tape for Steam Sterilization
K-Number: K260181 · 2026-02-20
ApplicantIntertape Polymer Group
Decision Date2026-02-20
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
LF Process Indicator Tape for Steam Sterilization is a medical device manufactured by Intertape Polymer Group. It received FDA 510(k) clearance on 2026-02-20 under approval number K260181. 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 LF Process Indicator Tape for Steam Sterilization?
LF Process Indicator Tape for Steam Sterilization is a medical device that received FDA 510(k) clearance on 2026-02-20. It is manufactured by Intertape Polymer Group. The 510(k) number is K260181.
When was LF Process Indicator Tape for Steam Sterilization approved by the FDA?
LF Process Indicator Tape for Steam Sterilization received FDA 510(k) clearance on 2026-02-20, under approval number K260181.
What company makes LF Process Indicator Tape for Steam Sterilization?
LF Process Indicator Tape for Steam Sterilization is manufactured by Intertape Polymer Group.
What is the FDA product code for LF Process Indicator Tape for Steam Sterilization?
The FDA product code for LF Process Indicator Tape for Steam Sterilization is JOJ.
Related PubMed Literature
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.