Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL

K-Number: K932643 · 1993-07-08

ApplicantBio-Rad
Decision Date1993-07-08
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LYPHOCHEK(R) URINE TOXICOLOGY SCREEN-LOW CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K932643. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 319 devices →

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.

↑