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FDA 510(k)

LARYNGOSCOPE

K-Number: K912905 · 1991-09-30

ApplicantAcorn Group, Inc.
Decision Date1991-09-30
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Acorn Group, Inc.. It received FDA 510(k) clearance on 1991-09-30 under 510(k) number K912905. 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?

LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1991-09-30. The listed applicant is Acorn Group, Inc.. The 510(k) number is K912905.

When did LARYNGOSCOPE receive FDA 510(k) clearance?

LARYNGOSCOPE received FDA 510(k) clearance on 1991-09-30, under 510(k) number K912905.

Who is the listed applicant for LARYNGOSCOPE?

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

What is the FDA product code for LARYNGOSCOPE?

The FDA product code for LARYNGOSCOPE is CCW.

Related Clinical Trials

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Other records listing Acorn Group, 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.

K914362TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWSK904126VISIRASERK900430IRRIGATION AND SUCTION APPARATUS

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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