Chemiluminescence LH

FDA 510(k) K935319 · Nichols Institute Diagnostics

Substantially Equivalent

510(k) numberK935319

Submission

Device name
Chemiluminescence LH
Applicant
Nichols Institute Diagnostics
San Juan Capistrano, CA, US
Received
October 20, 1993
Decision date
April 5, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CEP – Radioimmunoassay, Luteinizing Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1485
Specialty
Clinical Chemistry

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Questions and answers

When was Chemiluminescence LH cleared by the FDA?

Chemiluminescence LH (K935319) received a 510(k) decision of Substantially Equivalent on April 5, 1995, 532 days after the submission was received.

What is the product code of K935319?

The FDA product code is CEP – Radioimmunoassay, Luteinizing Hormone, a Class I (low risk) device regulated under 21 CFR 862.1485.