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)

VMX MINI-LOG FLOWMETER

K-Number: K914126 · 1993-03-05

Decision Date1993-03-05
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VMX MINI-LOG FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Clement Clarke, Inc.. It received FDA 510(k) clearance on 1993-03-05 under 510(k) number K914126. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMX MINI-LOG FLOWMETER?

VMX MINI-LOG FLOWMETER is a medical device that received FDA 510(k) clearance on 1993-03-05. The listed applicant is Clement Clarke, Inc.. The 510(k) number is K914126.

When did VMX MINI-LOG FLOWMETER receive FDA 510(k) clearance?

VMX MINI-LOG FLOWMETER received FDA 510(k) clearance on 1993-03-05, under 510(k) number K914126.

Who is the listed applicant for VMX MINI-LOG FLOWMETER?

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

What is the FDA product code for VMX MINI-LOG FLOWMETER?

The FDA product code for VMX MINI-LOG FLOWMETER is BZH.

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 Clement Clarke, 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.

View all 10 devices →

Related Devices (Code: BZH)

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.

↑