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FDA 510(k)

EXACTA & CONNECTA STOPCOCKS W/EXTENSION

K-Number: K823120 · 1982-11-08

Decision Date1982-11-08
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXACTA & CONNECTA STOPCOCKS W/EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Viggo, Inc.. It received FDA 510(k) clearance on 1982-11-08 under 510(k) number K823120. 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 EXACTA & CONNECTA STOPCOCKS W/EXTENSION?

EXACTA & CONNECTA STOPCOCKS W/EXTENSION is a medical device that received FDA 510(k) clearance on 1982-11-08. The listed applicant is Pioneer Viggo, Inc.. The 510(k) number is K823120.

When did EXACTA & CONNECTA STOPCOCKS W/EXTENSION receive FDA 510(k) clearance?

EXACTA & CONNECTA STOPCOCKS W/EXTENSION received FDA 510(k) clearance on 1982-11-08, under 510(k) number K823120.

Who is the listed applicant for EXACTA & CONNECTA STOPCOCKS W/EXTENSION?

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

What is the FDA product code for EXACTA & CONNECTA STOPCOCKS W/EXTENSION?

The FDA product code for EXACTA & CONNECTA STOPCOCKS W/EXTENSION 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 Pioneer Viggo, 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: 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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