MOORE TRACHEOSTOMY TUBE
K-Number: K962240 · 1996-08-15
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Device Summary
Frequently Asked Questions
What is the MOORE TRACHEOSTOMY TUBE?
MOORE TRACHEOSTOMY TUBE is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K962240.
When did MOORE TRACHEOSTOMY TUBE receive FDA 510(k) clearance?
MOORE TRACHEOSTOMY TUBE received FDA 510(k) clearance on 1996-08-15, under 510(k) number K962240.
Who is the listed applicant for MOORE TRACHEOSTOMY TUBE?
The FDA 510(k) record lists Boston Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOORE TRACHEOSTOMY TUBE?
The FDA product code for MOORE TRACHEOSTOMY TUBE 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 Boston Medical Products, 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: 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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