BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS)
K-Number: K902484 · 1990-06-21
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Device Summary
Frequently Asked Questions
What is the BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS)?
BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS) is a medical device that received FDA 510(k) clearance on 1990-06-21. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K902484.
When did BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS) receive FDA 510(k) clearance?
BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS) received FDA 510(k) clearance on 1990-06-21, under 510(k) number K902484.
Who is the listed applicant for BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS)?
The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS)?
The FDA product code for BECKMAN KAPPA LIGHT CHAIN REAGENT (ADD'L CLAIMS) is DFH.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Beckman Instruments, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DFH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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