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FDA 510(k)

DISPOSBLADE LARYNGOSCOPE

K-Number: K833133 · 1983-10-27

ApplicantGeller & Bozeman
Decision Date1983-10-27
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSBLADE LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Geller & Bozeman. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K833133. 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 DISPOSBLADE LARYNGOSCOPE?

DISPOSBLADE LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Geller & Bozeman. The 510(k) number is K833133.

When did DISPOSBLADE LARYNGOSCOPE receive FDA 510(k) clearance?

DISPOSBLADE LARYNGOSCOPE received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833133.

Who is the listed applicant for DISPOSBLADE LARYNGOSCOPE?

The FDA 510(k) record lists Geller & Bozeman as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSBLADE LARYNGOSCOPE?

The FDA product code for DISPOSBLADE LARYNGOSCOPE 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

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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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