FDA 510(k)

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)

N.º K: K233187 · 2023-10-27

SolicitanteSteris

Fecha de decisión2023-10-27

Código de productoJOJ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2023-10-27 under 510(k) number K233187. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is Steris. The 510(k) number is K233187.

When did Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) receive FDA 510(k) clearance?

Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) received FDA 510(k) clearance on 2023-10-27, under 510(k) number K233187.

Who is the listed applicant for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

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

What is the FDA product code for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078)?

The FDA product code for Celerity Vaporized VH2O2 Process Indicator Adhesive Label (PCC078) is JOJ.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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

Otros registros que enlistan a Steris como solicitante

K251452Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)K242773Electro Lube NXT K242189CELERITY HP Indicator Tape (PCC077)K241344MetriCide™ OPA Plus Solution Test Strip K241055Electro Lube NXT K240760CELERITY HP Indicator Tape

Ver todos los 19 dispositivos →

Dispositivos relacionados (Código: JOJ)

K2619923M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)Solventum US, LLC K260181LF Process Indicator Tape for Steam SterilizationIntertape Polymer Group K251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA Test StripsSerim Research K251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118STERIS Corporation K243876VERIFY STEAM Integrating IndicatorSTERIS Corporation

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.