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MODEL TP THERMISTOR PROBE

K831528 Class II Traditional
Decision Date
1983-06-30
Sponsor / Applicant
Scimed Life Systems, Inc.

Technical Specification

510(k) Submission ID K831528
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 1983-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL TP THERMISTOR PROBE received FDA 510(k) clearance under submission number K831528, sponsored by Scimed Life Systems, 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 1983-06-30.

Classification & Regulation

This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.