Terragene® Bionova® BT20 Biological Indicator

FDA 510(k) K251122 · Terragene

Substantially Equivalent

510(k) numberK251122

Submission

Device name
Terragene® Bionova® BT20 Biological Indicator
Applicant
Terragene
Alvear, AR
Received
April 11, 2025
Decision date
August 4, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRC – Indicator, Biological Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

Other 510(k)s with product code FRC

510(k)DeviceApplicantDecision
K260766Celerity 5 HP Biological Indicator (LCB052)FRC · Special STERIS Corporation04/08/2026SE
K252680Celerity™ 20 HP Biological IndicatorFRC · Special STERIS Corporation09/24/2025SE
K251452Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059)…FRC · Special Steris06/06/2025SE
K250061Celerity IncubatorFRC · Special STERIS Corporation02/06/2025SE
K250044Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059)…FRC · Special STERIS Corporation02/06/2025SE
K2435013M™ Attest™ Super Rapid Steam Extended Cycle Clear Challenge Pack 1492PCDE; 3M™ Attest™…FRC · Traditional 3M Company01/28/2025SE
K242453Terragene® Bionova® Photon Process Challenge Device with unique-point integrator…FRC · Traditional Terragene S.A.12/12/2024SE
K2425383M™ Attest™ Super Rapid Readout Biological Indicator 1493; 3M™ Attest™ Super Rapid Steam…FRC · Traditional 3M Company11/25/2024SE
K2419593M™ Attest™ Super Rapid Steam Clear Challenge Pack (1492PCD); 3M™ Attest™ Auto-reader…FRC · Traditional 3M Company10/18/2024SE
K231383Terragene® Bionova® Self-Contained Biological Indicator (BT95), Terragene® Bionova®…FRC · Traditional Terragene S.A.09/18/2024SE

Questions and answers

When was Terragene® Bionova® BT20 Biological Indicator cleared by the FDA?

Terragene® Bionova® BT20 Biological Indicator (K251122) received a 510(k) decision of Substantially Equivalent on August 4, 2025, 115 days after the submission was received.

What is the product code of K251122?

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