BOBBIN STYLE VENTURI VENT TUBE
K-Number: K943847 · 1994-09-02
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Device Summary
Frequently Asked Questions
What is the BOBBIN STYLE VENTURI VENT TUBE?
BOBBIN STYLE VENTURI VENT TUBE is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Micromed Development Corp.. The 510(k) number is K943847.
When did BOBBIN STYLE VENTURI VENT TUBE receive FDA 510(k) clearance?
BOBBIN STYLE VENTURI VENT TUBE received FDA 510(k) clearance on 1994-09-02, under 510(k) number K943847.
Who is the listed applicant for BOBBIN STYLE VENTURI VENT TUBE?
The FDA 510(k) record lists Micromed Development Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOBBIN STYLE VENTURI VENT TUBE?
The FDA product code for BOBBIN STYLE VENTURI VENT TUBE is ETD.
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 Micromed Development Corp. 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: ETD)
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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