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SIMULATOR

K854265 Class I Traditional
Decision Date
1986-03-18
Sponsor / Applicant
Cygnus of South Florida, Inc.

Technical Specification

510(k) Submission ID K854265
Product Code JQP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2100
Decision Date 1986-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMULATOR received FDA 510(k) clearance under submission number K854265, sponsored by Cygnus of South Florida, 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 1986-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code JQP and 21 CFR 862.2100, within the Clinical Chemistry review panel as a Class I device.