LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL
K-Number: K932643 · 1993-07-08
Advertisement
Device Summary
Frequently Asked Questions
What is the LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL?
LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Bio-Rad. The 510(k) number is K932643.
When did LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL receive FDA 510(k) clearance?
LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL received FDA 510(k) clearance on 1993-07-08, under 510(k) number K932643.
Who is the listed applicant for LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW 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(R) URINE TOXICOLOGY SCREEN-LOW CONTROL?
The FDA product code for LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW 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.
Advertisement