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FDA 510(k)

MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE

K-Number: K962688 · 1996-07-25

ApplicantBoston Medical Products, Inc.
Decision Date1996-07-25
Product CodeKCF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MONTGOMERY RADIOPAQUE 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 1996-07-25 under 510(k) number K962688. 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 MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE?

MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K962688.

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

MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE received FDA 510(k) clearance on 1996-07-25, under 510(k) number K962688.

Who is the listed applicant for MONTGOMERY RADIOPAQUE 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 MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE?

The FDA product code for MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE is KCF.

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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.

K091135RUTTER SUPRA STOMAL STENTSK972317MONTGOMERY THYROPLASTY IMPLANT SYSTEMK972459RHINOCELL NASAL PACKINGSK972096BIVALVE NASAL SPLINTK972078POST-STOP EPISTAXIS CATHETERK972092NASAL AIRWAY SPLINT

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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.

K923355PHARYNGEAL SALIVARY BYPASS TUBEBoston Medical Products, Inc.K812305MONTG. ESOPHAGEAL -SALIVARY BYPASS- TUBEBoston Medical Products, Inc.

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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