ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5
K-Number: K872913 · 1987-09-10
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Device Summary
Frequently Asked Questions
What is the ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5?
ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5 is a medical device that received FDA 510(k) clearance on 1987-09-10. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K872913.
When did ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5 receive FDA 510(k) clearance?
ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5 received FDA 510(k) clearance on 1987-09-10, under 510(k) number K872913.
Who is the listed applicant for ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5?
The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5?
The FDA product code for ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5 is DGC.
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 Diagnostic Products 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: DGC)
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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