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FDA 510(k)

SENSOR-TIP TROCAR

K-Number: K933724 · 1993-12-27

ApplicantOrigin Medsystems, Inc.
Decision Date1993-12-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SENSOR-TIP TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1993-12-27 under 510(k) number K933724. 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 SENSOR-TIP TROCAR?

SENSOR-TIP TROCAR is a medical device that received FDA 510(k) clearance on 1993-12-27. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K933724.

When did SENSOR-TIP TROCAR receive FDA 510(k) clearance?

SENSOR-TIP TROCAR received FDA 510(k) clearance on 1993-12-27, under 510(k) number K933724.

Who is the listed applicant for SENSOR-TIP TROCAR?

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

What is the FDA product code for SENSOR-TIP TROCAR?

The FDA product code for SENSOR-TIP TROCAR is GCJ.

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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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