Dimension EXL LOCI BRAHMS Procalcitonin (PCT)
FDA 510(k) K220262 · Siemens Healthcare Diagnostics, Inc.
510(k) numberK220262
Submission
- Device name
- Dimension EXL LOCI BRAHMS Procalcitonin (PCT)
- Applicant
- Siemens Healthcare Diagnostics, Inc.
Newark, DE, US - Received
- January 31, 2022
- Decision date
- August 26, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- PRI – Procalcitonin Assay
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3215
- Specialty
- Microbiology
To aid in decision making on antibiotic therapy, including antibiotic initiation and discontinuation, for inpatients or patients in the Emergency Department, with suspected or confirmed lower respiratory tract infections (LRTI) defined as community-acquired pneumonia (CAP), acute bronchitis, and acute exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD).
Other 510(k)s with product code PRI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K192815 | Elecsys BRAHMS PCTPRI · Traditional | Roche Diagnostics | 03/09/2020SE |
| K173927 | Elecsys BRAHMS PCTPRI · Traditional | Roche Diagnostics | 07/06/2018SE |
| K173683 | LIAISON BRAHMS PCT II GEN, LIAISON Control BRAHMS PCT II GEN, LIAISON BRAHMS PCT II GEN…PRI · Traditional | DiaSorin, Inc. | 02/27/2018SE |
| K172713 | Lumipulse G BRAHMS PCT Immunoreaction Cartridges, Lumipulse G BRAHMS PCT…PRI · Traditional | Fujirebio Diagnostics,Inc. | 12/10/2017SE |
| K170652 | ARCHITECT B.R.A.H.M.S PCT, ARCHITECT B.R.A.H.M.S PCT Calibrators, ARCHITECT B.R.A.H.M.S…PRI · Traditional | Fisher Diagnostics | 06/01/2017SE |
| K171338 | B R A H M S PCT sensitive KRYPTORPRI · Traditional | Brahms GmbH | 05/31/2017SE |
| K162827 | Vidas B.R.A.H.M.S. PCT (PCT)PRI · Traditional | bioMerieux, Inc. | 02/23/2017SE |
More from bioMerieux, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K253528 | Atellica IM CA 19-9 IINIG · Traditional | 08/10/2026SE |
| K261364 | Atellica CH Acetaminophen 2 (ACTM)LDP · Traditional | 07/24/2026SE |
| K251998 | Atellica CH Diazo Total Bilirubin (D_TBil)CIG · Traditional | 02/27/2026SE |
| K251543 | Atellica® IM TSH3-Ultra II (TSH3ULII)JLW · Traditional | 02/06/2026SE |
| K251630 | Atellica IM Total PSA II (tPSAII)LTJ · Traditional | 01/05/2026SE |
| K250816 | ADVIA Centaur Anti-Thyroglobulin II (aTgII)JNL · Traditional | 12/04/2025SE |
| K250250 | ADVIA Centaur Anti-Thyroid Peroxidase IIJZO · Traditional | 10/17/2025SE |
| K242981 | Atellica IM Thyroglobulin (Tg)MSW · Traditional | 06/20/2025SE |
| K243570 | Dimension LOCI Thyroid Stimulating Hormone Flex reagent cartridge (TSHL); Dimension LOCI…JLW · Traditional | 04/25/2025SE |
| K242685 | Atellica® CH Creatinine_3 (Crea3)CGX · Traditional | 12/04/2024SE |
Questions and answers
When was Dimension EXL LOCI BRAHMS Procalcitonin (PCT) cleared by the FDA?
Dimension EXL LOCI BRAHMS Procalcitonin (PCT) (K220262) received a 510(k) decision of Substantially Equivalent on August 26, 2022, 207 days after the submission was received.
What is the product code of K220262?
The FDA product code is PRI – Procalcitonin Assay, a Class II (moderate risk) device regulated under 21 CFR 866.3215.