IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6
K-Number: K991094 · 1999-05-13
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Device Summary
Frequently Asked Questions
What is the IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6?
IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6 is a medical device that received FDA 510(k) clearance on 1999-05-13. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K991094.
When did IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6 receive FDA 510(k) clearance?
IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6 received FDA 510(k) clearance on 1999-05-13, under 510(k) number K991094.
Who is the listed applicant for IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6?
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 IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6?
The FDA product code for IMMULITE 2000 ANTI-TG AB, MODEL L2KTG2, L2KTG6 is JZO.
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: JZO)
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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