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FDA 510(k)

MOORE TRACHEOSTOMY TUBE

K-Number: K962240 · 1996-08-15

Decision Date1996-08-15
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOORE TRACHEOSTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Products, Inc.. It received FDA 510(k) clearance on 1996-08-15 under 510(k) number K962240. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 33 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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