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FDA 510(k)

Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape

K-Number: K161024 · 2016-06-28

ApplicantCanadian Technical Tape, Ltd.
Decision Date2016-06-28
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape is a medical device manufactured by Canadian Technical Tape, Ltd.. It received FDA 510(k) clearance on 2016-06-28 under approval number K161024. 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 Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape?

Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape is a medical device that received FDA 510(k) clearance on 2016-06-28. It is manufactured by Canadian Technical Tape, Ltd.. The 510(k) number is K161024.

When was Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape approved by the FDA?

Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape received FDA 510(k) clearance on 2016-06-28, under approval number K161024.

What company makes Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape?

Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape is manufactured by Canadian Technical Tape, Ltd..

What is the FDA product code for Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape?

The FDA product code for Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape is JOJ.

Related Clinical Trials

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Related PubMed Literature

PMID: 41987831 From Concept to Clinic: Pre-Clinical Testing and Regulatory Considerations in Spine Implant Development. JOR spine (2026) PMID: 40237623 Diffusion of Hydrogen Peroxide Through Medical Grade Poly(Ether)urethane: Analyzing Mechanisms of Sorption and Transport to Support Sterilization With Vapor Phase Hydrogen Peroxide. Journal of biomedical materials research. Part B, Applied biomaterials (2025) PMID: 39961588 The use of predetermined change control plans to enable the release of new versions of software as a medical device. Expert review of medical devices (2025)

Related Devices (Code: JOJ)

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. K170426AN85/AN86 EO IndicatorsAndersen 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.

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