ORIGIN SECONDARY CANNULA AND TROCAR
K-Number: K922460 · 1992-09-16
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Device Summary
Frequently Asked Questions
What is the ORIGIN SECONDARY CANNULA AND TROCAR?
ORIGIN SECONDARY CANNULA AND TROCAR is a medical device that received FDA 510(k) clearance on 1992-09-16. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K922460.
When did ORIGIN SECONDARY CANNULA AND TROCAR receive FDA 510(k) clearance?
ORIGIN SECONDARY CANNULA AND TROCAR received FDA 510(k) clearance on 1992-09-16, under 510(k) number K922460.
Who is the listed applicant for ORIGIN SECONDARY CANNULA AND 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 SECONDARY CANNULA AND TROCAR?
The FDA product code for ORIGIN SECONDARY CANNULA AND TROCAR is GEA.
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.
Related Devices (Code: GEA)
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.
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