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FDA 510(k)

BLUNT TIP TROCAR PORT

K-Number: K992353 · 1999-07-30

ApplicantOrigin Medsystems, Inc.
Decision Date1999-07-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLUNT TIP TROCAR PORT 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 1999-07-30 under 510(k) number K992353. 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 BLUNT TIP TROCAR PORT?

BLUNT TIP TROCAR PORT is a medical device that received FDA 510(k) clearance on 1999-07-30. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K992353.

When did BLUNT TIP TROCAR PORT receive FDA 510(k) clearance?

BLUNT TIP TROCAR PORT received FDA 510(k) clearance on 1999-07-30, under 510(k) number K992353.

Who is the listed applicant for BLUNT TIP TROCAR PORT?

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 BLUNT TIP TROCAR PORT?

The FDA product code for BLUNT TIP TROCAR PORT 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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