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BIOCELL SPINAL FLUID CONTROL

K830179 Class I Traditional
Decision Date
1983-02-18
Sponsor / Applicant
Biocell Laboratories, Inc.

Technical Specification

510(k) Submission ID K830179
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1983-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOCELL SPINAL FLUID CONTROL received FDA 510(k) clearance under submission number K830179, sponsored by Biocell Laboratories, 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 1983-02-18.

Classification & Regulation

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