FDA 510(k)

Celerity™ 20 HP Biological Indicator

Número K: K252680 · 2025-09-24

Data da decisão2025-09-24

Código do produtoFRC

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Celerity™ 20 HP Biological Indicator is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2025-09-24 under 510(k) number K252680. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Celerity™ 20 HP Biological Indicator?

Celerity™ 20 HP Biological Indicator is a medical device that received FDA 510(k) clearance on 2025-09-24. The listed applicant is STERIS Corporation. The 510(k) number is K252680.

When did Celerity™ 20 HP Biological Indicator receive FDA 510(k) clearance?

Celerity™ 20 HP Biological Indicator received FDA 510(k) clearance on 2025-09-24, under 510(k) number K252680.

Who is the listed applicant for Celerity™ 20 HP Biological Indicator?

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

What is the FDA product code for Celerity™ 20 HP Biological Indicator?

The FDA product code for Celerity™ 20 HP Biological Indicator is FRC.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Outros registros que listam STERIS Corporation como candidato(a)

K261055AMSCO 700 Steam Sterilizer K260766Celerity 5 HP Biological Indicator (LCB052)K251666SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 K251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118 K243876VERIFY STEAM Integrating Indicator K250842PADLOCK CLIP EFTR Kit (00713229)

Ver todos os 120 dispositivos →

Dispositivos Relacionados (Código: FRC)

K260766Celerity 5 HP Biological Indicator (LCB052)STERIS Corporation K251122Terragene® Bionova® BT20 Biological IndicatorTerragene K251452Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)Steris K250061Celerity IncubatorSTERIS Corporation K250044Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)STERIS Corporation K2435013M® Attest® Super Rapid Steam Extended Cycle Clear Challenge Pack 1492PCDE; 3M® Attest® Auto-reader 490; 3M® Attest® Auto-reader 490H; 3M® Attest® Mini Auto-reader 490M3M Company

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.