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FDA 510(k)

VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES

K-Number: K071976 · 2007-09-06

ApplicantVectec
Decision Date2007-09-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Vectec. It received FDA 510(k) clearance on 2007-09-06 under 510(k) number K071976. 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 TROCARS AND LAPAROSCOPIC ACCESSORIES?

VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES is a medical device that received FDA 510(k) clearance on 2007-09-06. The listed applicant is Vectec. The 510(k) number is K071976.

When did VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES receive FDA 510(k) clearance?

VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES received FDA 510(k) clearance on 2007-09-06, under 510(k) number K071976.

Who is the listed applicant for VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES?

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 TROCARS AND LAPAROSCOPIC ACCESSORIES?

The FDA product code for VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES 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.

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.

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.

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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