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FDA 510(k)

LARYNGOSCOPE BLADES/HANDLES & LAMPS

K-Number: K833055 · 1983-11-14

Decision Date1983-11-14
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE BLADES/HANDLES & LAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Medovations, Inc.. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833055. 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 LARYNGOSCOPE BLADES/HANDLES & LAMPS?

LARYNGOSCOPE BLADES/HANDLES & LAMPS is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Medovations, Inc.. The 510(k) number is K833055.

When did LARYNGOSCOPE BLADES/HANDLES & LAMPS receive FDA 510(k) clearance?

LARYNGOSCOPE BLADES/HANDLES & LAMPS received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833055.

Who is the listed applicant for LARYNGOSCOPE BLADES/HANDLES & LAMPS?

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

What is the FDA product code for LARYNGOSCOPE BLADES/HANDLES & LAMPS?

The FDA product code for LARYNGOSCOPE BLADES/HANDLES & LAMPS 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.

Other records listing Medovations, 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.

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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.

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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