Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SURGICAL TROCAR AND TROCAR SLEEVE

K-Number: K932229 · 1993-08-18

Decision Date1993-08-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGICAL TROCAR AND TROCAR SLEEVE 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 1993-08-18 under 510(k) number K932229. 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 SURGICAL TROCAR AND TROCAR SLEEVE?

SURGICAL TROCAR AND TROCAR SLEEVE is a medical device that received FDA 510(k) clearance on 1993-08-18. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K932229.

When did SURGICAL TROCAR AND TROCAR SLEEVE receive FDA 510(k) clearance?

SURGICAL TROCAR AND TROCAR SLEEVE received FDA 510(k) clearance on 1993-08-18, under 510(k) number K932229.

Who is the listed applicant for SURGICAL TROCAR AND TROCAR SLEEVE?

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 SURGICAL TROCAR AND TROCAR SLEEVE?

The FDA product code for SURGICAL TROCAR AND TROCAR SLEEVE is GCJ.

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 Origin Medsystems, Inc. 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.

View all 50 devices →

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.

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.

↑