FOUR LUMEN BLAKEMORE TUBE
K-Number: K832672 · 1983-09-12
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Device Summary
Frequently Asked Questions
What is the FOUR LUMEN BLAKEMORE TUBE?
FOUR LUMEN BLAKEMORE TUBE is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Inmed Corp.. The 510(k) number is K832672.
When did FOUR LUMEN BLAKEMORE TUBE receive FDA 510(k) clearance?
FOUR LUMEN BLAKEMORE TUBE received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832672.
Who is the listed applicant for FOUR LUMEN BLAKEMORE TUBE?
The FDA 510(k) record lists Inmed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOUR LUMEN BLAKEMORE TUBE?
The FDA product code for FOUR LUMEN BLAKEMORE TUBE is KNT.
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 Inmed 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: KNT)
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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