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FDA 510(k)

MONTGOMERY RADIOPAQUE LARYNGEAL KEEL

K-Number: K962693 · 1996-08-09

ApplicantBoston Medical Products, Inc.
Decision Date1996-08-09
Product CodeFWN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MONTGOMERY RADIOPAQUE LARYNGEAL KEEL 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 1996-08-09 under 510(k) number K962693. The device is classified under product code FWN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONTGOMERY RADIOPAQUE LARYNGEAL KEEL?

MONTGOMERY RADIOPAQUE LARYNGEAL KEEL is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K962693.

When did MONTGOMERY RADIOPAQUE LARYNGEAL KEEL receive FDA 510(k) clearance?

MONTGOMERY RADIOPAQUE LARYNGEAL KEEL received FDA 510(k) clearance on 1996-08-09, under 510(k) number K962693.

Who is the listed applicant for MONTGOMERY RADIOPAQUE LARYNGEAL KEEL?

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 LARYNGEAL KEEL?

The FDA product code for MONTGOMERY RADIOPAQUE LARYNGEAL KEEL is FWN.

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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: FWN)

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 STENTSBoston Medical Products, Inc.K000154ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1E. Benson Hood Lab, Inc.K896667LORENZ STENTWalter Lorenz Surgical, Inc.K884810SILICONE LARYNGEAL STENTHood LaboratoriesK864936'EXMOOR' DAS GUPTA LARYNGEAL KEELExmoor Plastics , Ltd.K853726LARYNGEALHood Laboratories

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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