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TAP Blood Collection Device

K190225 Class II Traditional
Decision Date
2019-11-05
Sponsor / Applicant
Seventh Sense Biosystems, Inc.

Technical Specification

510(k) Submission ID K190225
Product Code PRJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 2019-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAP Blood Collection Device received FDA 510(k) clearance under submission number K190225, sponsored by Seventh Sense Biosystems, Inc.. 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 2019-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code PRJ and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.