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FDA 510(k)

DISPOSA-LITE LARYNGOSCOPE BLADE

K-Number: K832984 · 1983-10-28

ApplicantMichael S. Upsher
Decision Date1983-10-28
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSA-LITE LARYNGOSCOPE BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Michael S. Upsher. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K832984. 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 DISPOSA-LITE LARYNGOSCOPE BLADE?

DISPOSA-LITE LARYNGOSCOPE BLADE is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Michael S. Upsher. The 510(k) number is K832984.

When did DISPOSA-LITE LARYNGOSCOPE BLADE receive FDA 510(k) clearance?

DISPOSA-LITE LARYNGOSCOPE BLADE received FDA 510(k) clearance on 1983-10-28, under 510(k) number K832984.

Who is the listed applicant for DISPOSA-LITE LARYNGOSCOPE BLADE?

The FDA 510(k) record lists Michael S. Upsher as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSA-LITE LARYNGOSCOPE BLADE?

The FDA product code for DISPOSA-LITE LARYNGOSCOPE BLADE is CCW.

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.

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Other records listing Michael S. Upsher 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.

K832650UPSHER FIBERBRITE LARYNGOSCOPE

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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