REPROCESSED DISPOSABLE TROCARS
K-Number: K013987 · 2002-03-01
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Device Summary
Frequently Asked Questions
What is the REPROCESSED DISPOSABLE TROCARS?
REPROCESSED DISPOSABLE TROCARS is a medical device that received FDA 510(k) clearance on 2002-03-01. The listed applicant is Adven Medical. The 510(k) number is K013987.
When did REPROCESSED DISPOSABLE TROCARS receive FDA 510(k) clearance?
REPROCESSED DISPOSABLE TROCARS received FDA 510(k) clearance on 2002-03-01, under 510(k) number K013987.
Who is the listed applicant for REPROCESSED DISPOSABLE TROCARS?
The FDA 510(k) record lists Adven Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REPROCESSED DISPOSABLE TROCARS?
The FDA product code for REPROCESSED DISPOSABLE TROCARS is KBG.
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 Adven Medical 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: KBG)
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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