TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).
K-Number: K955461 · 1997-03-19
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Device Summary
Frequently Asked Questions
What is the TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).?
TRANSTRACHEAL CATHETER (ACC. RAVUSSIN). is a medical device that received FDA 510(k) clearance on 1997-03-19. The listed applicant is VBM Medizintechnik GmbH. The 510(k) number is K955461.
When did TRANSTRACHEAL CATHETER (ACC. RAVUSSIN). receive FDA 510(k) clearance?
TRANSTRACHEAL CATHETER (ACC. RAVUSSIN). received FDA 510(k) clearance on 1997-03-19, under 510(k) number K955461.
Who is the listed applicant for TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).?
The FDA 510(k) record lists VBM Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).?
The FDA product code for TRANSTRACHEAL CATHETER (ACC. RAVUSSIN). is BTO.
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 VBM Medizintechnik GmbH 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: BTO)
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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