Micromedic LH & FSH Ria Kit

FDA 510(k) K840188 · Micromedic Systems

Substantially Equivalent

510(k) numberK840188

Submission

Device name
Micromedic LH & FSH Ria Kit
Applicant
Micromedic Systems
Mchenry, IL, US
Received
January 18, 1984
Decision date
March 23, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Micromedic LH & FSH Ria Kit cleared by the FDA?

Micromedic LH & FSH Ria Kit (K840188) received a 510(k) decision of Substantially Equivalent on March 23, 1984, 65 days after the submission was received.

What is the product code of K840188?

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