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FDA 510(k)

PHARYNGEAL SALIVARY BYPASS TUBE

K-Number: K923355 · 1992-10-06

Decision Date1992-10-06
Product CodeKCF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHARYNGEAL SALIVARY BYPASS 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 1992-10-06 under 510(k) number K923355. The device is classified under product code KCF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARYNGEAL SALIVARY BYPASS TUBE?

PHARYNGEAL SALIVARY BYPASS TUBE is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K923355.

When did PHARYNGEAL SALIVARY BYPASS TUBE receive FDA 510(k) clearance?

PHARYNGEAL SALIVARY BYPASS TUBE received FDA 510(k) clearance on 1992-10-06, under 510(k) number K923355.

Who is the listed applicant for PHARYNGEAL SALIVARY BYPASS 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 PHARYNGEAL SALIVARY BYPASS TUBE?

The FDA product code for PHARYNGEAL SALIVARY BYPASS TUBE is KCF.

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: KCF)

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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