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T12S TELEMETRY TRANSMITTER

K081800 Class II Abbreviated
Decision Date
2008-09-24
Sponsor / Applicant
Mortara Instrument, Inc.

Technical Specification

510(k) Submission ID K081800
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2008-09-24
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T12S TELEMETRY TRANSMITTER received FDA 510(k) clearance under submission number K081800, sponsored by Mortara Instrument, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.