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FDA 510(k)

MECTRA TROCAR

K-Number: K934547 · 1994-02-18

ApplicantMectra Labs, Inc.
Decision Date1994-02-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MECTRA TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Mectra Labs, Inc.. It received FDA 510(k) clearance on 1994-02-18 under 510(k) number K934547. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MECTRA TROCAR?

MECTRA TROCAR is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Mectra Labs, Inc.. The 510(k) number is K934547.

When did MECTRA TROCAR receive FDA 510(k) clearance?

MECTRA TROCAR received FDA 510(k) clearance on 1994-02-18, under 510(k) number K934547.

Who is the listed applicant for MECTRA TROCAR?

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

What is the FDA product code for MECTRA TROCAR?

The FDA product code for MECTRA TROCAR is GCJ.

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Other records listing Mectra Labs, Inc. as applicant

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Related Devices (Code: GCJ)

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

View on FDA Database →

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

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