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FDA 510(k)

ORIGIN BLUNT TIP SURGICAL TROCAR

K-Number: K924011 · 1993-07-09

ApplicantOrigin Medsystems, Inc.
Decision Date1993-07-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ORIGIN BLUNT TIP SURGICAL 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 1993-07-09 under 510(k) number K924011. 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 ORIGIN BLUNT TIP SURGICAL TROCAR?

ORIGIN BLUNT TIP SURGICAL TROCAR is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K924011.

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

ORIGIN BLUNT TIP SURGICAL TROCAR received FDA 510(k) clearance on 1993-07-09, under 510(k) number K924011.

Who is the listed applicant for ORIGIN BLUNT TIP SURGICAL 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 ORIGIN BLUNT TIP SURGICAL TROCAR?

The FDA product code for ORIGIN BLUNT TIP SURGICAL 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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