LD-L REAGENT
K-Number: K851996 · 1985-05-31
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Device Summary
Frequently Asked Questions
What is the LD-L REAGENT?
LD-L REAGENT is a medical device that received FDA 510(k) clearance on 1985-05-31. The listed applicant is Alpkem Corp.. The 510(k) number is K851996.
When did LD-L REAGENT receive FDA 510(k) clearance?
LD-L REAGENT received FDA 510(k) clearance on 1985-05-31, under 510(k) number K851996.
Who is the listed applicant for LD-L REAGENT?
The FDA 510(k) record lists Alpkem Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LD-L REAGENT?
The FDA product code for LD-L REAGENT is CFJ.
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 Alpkem Corp. 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: CFJ)
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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