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)

MULTIPLE (IZON URINE COLLECTION KIT)

K-Number: K950246 · 1995-03-21

Decision Date1995-03-21
Product CodeJXA
Advisory CommitteeMI
DecisionUnknown

Device Summary

MULTIPLE (IZON URINE COLLECTION KIT) is the device name listed in this FDA 510(k) record. The listed applicant is Izon Business Products, Inc.. It received FDA 510(k) clearance on 1995-03-21 under 510(k) number K950246. The device is classified under product code JXA. It was reviewed by the MI advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MULTIPLE (IZON URINE COLLECTION KIT)?

MULTIPLE (IZON URINE COLLECTION KIT) is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Izon Business Products, Inc.. The 510(k) number is K950246.

When did MULTIPLE (IZON URINE COLLECTION KIT) receive FDA 510(k) clearance?

MULTIPLE (IZON URINE COLLECTION KIT) received FDA 510(k) clearance on 1995-03-21, under 510(k) number K950246.

Who is the listed applicant for MULTIPLE (IZON URINE COLLECTION KIT)?

The FDA 510(k) record lists Izon Business Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE (IZON URINE COLLECTION KIT)?

The FDA product code for MULTIPLE (IZON URINE COLLECTION KIT) is JXA.

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 Izon Business Products, Inc. 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: JXA)

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.

↑