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)

CHEMSTRIP URINE ANALYZER

K-Number: K931602 · 1993-06-15

Decision Date1993-06-15
Product CodeKQO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHEMSTRIP URINE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1993-06-15 under 510(k) number K931602. The device is classified under product code KQO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMSTRIP URINE ANALYZER?

CHEMSTRIP URINE ANALYZER is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K931602.

When did CHEMSTRIP URINE ANALYZER receive FDA 510(k) clearance?

CHEMSTRIP URINE ANALYZER received FDA 510(k) clearance on 1993-06-15, under 510(k) number K931602.

Who is the listed applicant for CHEMSTRIP URINE ANALYZER?

The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEMSTRIP URINE ANALYZER?

The FDA product code for CHEMSTRIP URINE ANALYZER is KQO.

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 Boehringer Mannheim 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.

View all 340 devices →

Related Devices (Code: KQO)

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.

↑