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MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE

K880740 Class II Traditional
Decision Date
1988-03-22
Sponsor / Applicant
Spectramed, Inc.

Technical Specification

510(k) Submission ID K880740
Product Code DQF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1670
Decision Date 1988-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE received FDA 510(k) clearance under submission number K880740, sponsored by Spectramed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code DQF and 21 CFR 870.1670, within the Cardiovascular review panel as a Class II device.