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FDA 510(k)

VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE

K-Number: K103707 · 2011-02-04

ApplicantVectec
Decision Date2011-02-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Vectec. It received FDA 510(k) clearance on 2011-02-04 under 510(k) number K103707. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE?

VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE is a medical device that received FDA 510(k) clearance on 2011-02-04. The listed applicant is Vectec. The 510(k) number is K103707.

When did VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE receive FDA 510(k) clearance?

VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE received FDA 510(k) clearance on 2011-02-04, under 510(k) number K103707.

Who is the listed applicant for VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE?

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

What is the FDA product code for VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE?

The FDA product code for VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE is GEI.

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.

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Other records listing Vectec 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.

K121370VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLEK071976VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES

Related Devices (Code: GEI)

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.

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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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