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FDA 510(k)

VIGGO CONNECTA 3-WAY INFUSION STOPCOCK

K-Number: K850280 · 1985-04-11

Decision Date1985-04-11
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIGGO CONNECTA 3-WAY INFUSION STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Viggo Products. It received FDA 510(k) clearance on 1985-04-11 under 510(k) number K850280. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIGGO CONNECTA 3-WAY INFUSION STOPCOCK?

VIGGO CONNECTA 3-WAY INFUSION STOPCOCK is a medical device that received FDA 510(k) clearance on 1985-04-11. The listed applicant is Viggo Products. The 510(k) number is K850280.

When did VIGGO CONNECTA 3-WAY INFUSION STOPCOCK receive FDA 510(k) clearance?

VIGGO CONNECTA 3-WAY INFUSION STOPCOCK received FDA 510(k) clearance on 1985-04-11, under 510(k) number K850280.

Who is the listed applicant for VIGGO CONNECTA 3-WAY INFUSION STOPCOCK?

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

What is the FDA product code for VIGGO CONNECTA 3-WAY INFUSION STOPCOCK?

The FDA product code for VIGGO CONNECTA 3-WAY INFUSION STOPCOCK is FMG.

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 Viggo 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.

View all 7 devices →

Related Devices (Code: FMG)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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