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)

VOSS VEIN CLAMP

K-Number: K885161 · 1989-12-22

Decision Date1989-12-22
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VOSS VEIN CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Voss Medical Products. It received FDA 510(k) clearance on 1989-12-22 under 510(k) number K885161. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOSS VEIN CLAMP?

VOSS VEIN CLAMP is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Voss Medical Products. The 510(k) number is K885161.

When did VOSS VEIN CLAMP receive FDA 510(k) clearance?

VOSS VEIN CLAMP received FDA 510(k) clearance on 1989-12-22, under 510(k) number K885161.

Who is the listed applicant for VOSS VEIN CLAMP?

The FDA 510(k) record lists Voss Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOSS VEIN CLAMP?

The FDA product code for VOSS VEIN CLAMP is DXC.

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 Voss Medical Products 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: DXC)

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.

↑