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SPINAL FLUID CONTROL(HUMAN)

K801854 Class I Traditional
Decision Date
1980-09-16
Sponsor / Applicant
Environmental Chemical Specialties

Technical Specification

510(k) Submission ID K801854
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1980-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPINAL FLUID CONTROL(HUMAN) received FDA 510(k) clearance under submission number K801854, sponsored by Environmental Chemical Specialties. 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 1980-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.