LF Process Indicator Tape for Steam Sterilization

FDA 510(k) K260181 · Intertape Polymer Group

Substantially Equivalent

510(k) numberK260181

Submission

Device name
LF Process Indicator Tape for Steam Sterilization
Applicant
Intertape Polymer Group
Sarasota, FL, US
Received
January 21, 2026
Decision date
February 20, 2026
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOJ – Indicator, Physical/Chemical Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

Other 510(k)s with product code JOJ

510(k)DeviceApplicantDecision
K251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure…JOJ · Traditional Shenzhen Safesecure Medical Infection Control…12/23/2025SE
K251035DISINTEK™ PA Test StripsJOJ · Traditional Serim Research06/03/2025SE
K251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118JOJ · Special STERIS Corporation05/02/2025SE
K243876VERIFY STEAM Integrating IndicatorJOJ · Special STERIS Corporation04/25/2025SE
K250172Green Card Bowie-Dick Test (BD115)JOJ · Special Steritec Products, Inc. (A Getinge Company)02/20/2025SE
K242860Type 5 Integrating Indicator for Steam (CSPN-15)JOJ · Traditional True Indicating, LLC01/17/2025SE
K241036Autoclave Indicator Tape; EO Indicator TapeJOJ · Traditional Jiangmen New Era External Use Drug Co., Ltd.12/17/2024SE
K243475Chemical Indicator for enspire CLCSPS (LCC015)JOJ · Special STERIS Corporation12/04/2024SE
K242795Getinge Assured MI Steam Migrating IntegratorJOJ · Special Steritec Products Mfg. (A Getinge Group Company)10/15/2024SE
K241836Kem Medical Lead-free Chemical Indicators for Steam SterilizationJOJ · Traditional Kem Medical Products Corporation09/30/2024SE

Questions and answers

When was LF Process Indicator Tape for Steam Sterilization cleared by the FDA?

LF Process Indicator Tape for Steam Sterilization (K260181) received a 510(k) decision of Substantially Equivalent on February 20, 2026, 30 days after the submission was received.

What is the product code of K260181?

The FDA product code is JOJ – Indicator, Physical/Chemical Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.