Model 250 Liquid Chromotagraphy Pump

FDA 510(k) K884886 · The Perkin-Elmer Corp.

Substantially Equivalent

510(k) numberK884886

Submission

Device name
Model 250 Liquid Chromotagraphy Pump
Applicant
The Perkin-Elmer Corp.
Norwalk, CT, US
Received
November 22, 1988
Decision date
February 2, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LDM – Instrumentation, High Pressure Liquid Chromatography
Device class
Class I (low risk)
Regulation
21 CFR 862.2260
Specialty
Clinical Chemistry

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Questions and answers

When was Model 250 Liquid Chromotagraphy Pump cleared by the FDA?

Model 250 Liquid Chromotagraphy Pump (K884886) received a 510(k) decision of Substantially Equivalent on February 2, 1989, 72 days after the submission was received.

What is the product code of K884886?

The FDA product code is LDM – Instrumentation, High Pressure Liquid Chromatography, a Class I (low risk) device regulated under 21 CFR 862.2260.