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FDA 510(k)

BAUMAN DISPOSABLE LARYNGOSCOPE BLADES

K-Number: K905273 · 1992-03-24

ApplicantVital Signs, Inc.
Decision Date1992-03-24
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BAUMAN DISPOSABLE LARYNGOSCOPE BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1992-03-24 under 510(k) number K905273. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUMAN DISPOSABLE LARYNGOSCOPE BLADES?

BAUMAN DISPOSABLE LARYNGOSCOPE BLADES is a medical device that received FDA 510(k) clearance on 1992-03-24. The listed applicant is Vital Signs, Inc.. The 510(k) number is K905273.

When did BAUMAN DISPOSABLE LARYNGOSCOPE BLADES receive FDA 510(k) clearance?

BAUMAN DISPOSABLE LARYNGOSCOPE BLADES received FDA 510(k) clearance on 1992-03-24, under 510(k) number K905273.

Who is the listed applicant for BAUMAN DISPOSABLE LARYNGOSCOPE BLADES?

The FDA 510(k) record lists Vital Signs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAUMAN DISPOSABLE LARYNGOSCOPE BLADES?

The FDA product code for BAUMAN DISPOSABLE LARYNGOSCOPE BLADES is CCW.

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Related Devices (Code: CCW)

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.

K191602APA Oxy BladeVenner Medical (Singapore) Pte, Ltd.K163412Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)Girgis Scope, LLCK121378AIRTRAQ SP AIRTRAQ AVANTProdol Meditec , Ltd.K063477NOVAMED MRI CONDITIONAL LARYNGOSCOPE SETNovamed, LLCK062523TRU-MR LARYNGOSCOPE SETTruphatek International, Ltd.K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002Minrad, 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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