LYPHOCHEK THERAPEUTIC DRUG CONTROL
K-Number: K833794 · 1984-01-24
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Device Summary
Frequently Asked Questions
What is the LYPHOCHEK THERAPEUTIC DRUG CONTROL?
LYPHOCHEK THERAPEUTIC DRUG CONTROL is a medical device that received FDA 510(k) clearance on 1984-01-24. The listed applicant is Bio-Rad. The 510(k) number is K833794.
When did LYPHOCHEK THERAPEUTIC DRUG CONTROL receive FDA 510(k) clearance?
LYPHOCHEK THERAPEUTIC DRUG CONTROL received FDA 510(k) clearance on 1984-01-24, under 510(k) number K833794.
Who is the listed applicant for LYPHOCHEK THERAPEUTIC DRUG CONTROL?
The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LYPHOCHEK THERAPEUTIC DRUG CONTROL?
The FDA product code for LYPHOCHEK THERAPEUTIC DRUG CONTROL is DIF.
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 Bio-Rad 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: DIF)
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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