Titanan Gel Serum Protein Electrophores

FDA 510(k) K821517 · Helena Laboratories

Substantially Equivalent

510(k) numberK821517

Submission

Device name
Titanan Gel Serum Protein Electrophores
Applicant
Helena Laboratories
Mchenry, IL, US
Received
May 21, 1982
Decision date
June 10, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJN – Apparatus, Electrophoresis, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2485
Specialty
Clinical Chemistry

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Questions and answers

When was Titanan Gel Serum Protein Electrophores cleared by the FDA?

Titanan Gel Serum Protein Electrophores (K821517) received a 510(k) decision of Substantially Equivalent on June 10, 1982, 20 days after the submission was received.

What is the product code of K821517?

The FDA product code is JJN – Apparatus, Electrophoresis, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2485.