meddevicedb.com FDA Device Reference

Atellica Solution, Atellica A-LYTE Integrated Multisensor Na+/K+/CI-, Atellica CH Albumin BCP Reagent (Alb_p), Atellica IM Thyroid Stimulating Hormone TSH, Atellica CH Vancomycin (Vanc)

K161954 Class II Traditional
Decision Date
2017-03-09
Sponsor / Applicant
Siemens Healthcare Diagnostics

Technical Specification

510(k) Submission ID K161954
Product Code JGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1665
Decision Date 2017-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Atellica Solution, Atellica A-LYTE Integrated Multisensor Na+/K+/CI-, Atellica CH Albumin BCP Reagent (Alb_p), Atellica IM Thyroid Stimulating Hormone TSH, Atellica CH Vancomycin (Vanc) received FDA 510(k) clearance under submission number K161954, sponsored by Siemens Healthcare Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2017-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code JGS and 21 CFR 862.1665, within the Clinical Chemistry review panel as a Class II device.