HDL Centrifikit

FDA 510(k) K781093 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK781093

Submission

Device name
HDL Centrifikit
Applicant
Beckman Instruments, Inc.
Mchenry, IL, US
Received
June 30, 1978
Decision date
August 14, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LBR – Ldl & Vldl Precipitation, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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Questions and answers

When was HDL Centrifikit cleared by the FDA?

HDL Centrifikit (K781093) received a 510(k) decision of Substantially Equivalent on August 14, 1978, 45 days after the submission was received.

What is the product code of K781093?

The FDA product code is LBR – Ldl & Vldl Precipitation, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.