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FDA 510(k)

LF Process Indicator Tape for Steam Sterilization

K-Number: K260181 · 2026-02-20

Decision Date2026-02-20
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LF Process Indicator Tape for Steam Sterilization is the device name listed in this FDA 510(k) record. The listed applicant is Intertape Polymer Group. It received FDA 510(k) clearance on 2026-02-20 under 510(k) 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. The listed applicant is Intertape Polymer Group. The 510(k) number is K260181.

When did LF Process Indicator Tape for Steam Sterilization receive FDA 510(k) clearance?

LF Process Indicator Tape for Steam Sterilization received FDA 510(k) clearance on 2026-02-20, under 510(k) number K260181.

Who is the listed applicant for LF Process Indicator Tape for Steam Sterilization?

The FDA 510(k) record lists Intertape Polymer Group as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: JOJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.