Beckman Lambda Light Chain Reagent (Add'L Claims)

FDA 510(k) K902485 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK902485

Submission

Device name
Beckman Lambda Light Chain Reagent (Add'L Claims)
Applicant
Beckman Instruments, Inc.
Brea, CA, US
Received
June 5, 1990
Decision date
June 21, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DEH – Lambda, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5550
Specialty
Immunology

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Questions and answers

When was Beckman Lambda Light Chain Reagent (Add'L Claims) cleared by the FDA?

Beckman Lambda Light Chain Reagent (Add'L Claims) (K902485) received a 510(k) decision of Substantially Equivalent on June 21, 1990, 16 days after the submission was received.

What is the product code of K902485?

The FDA product code is DEH – Lambda, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5550.