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FDA 510(k)

LARYNGOSTAT LARYNGOSCOPE HANDLE

K-Number: K895954 · 1989-10-30

ApplicantMichigan Instruments, Inc.
Decision Date1989-10-30
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSTAT LARYNGOSCOPE HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Michigan Instruments, Inc.. It received FDA 510(k) clearance on 1989-10-30 under 510(k) number K895954. 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 LARYNGOSTAT LARYNGOSCOPE HANDLE?

LARYNGOSTAT LARYNGOSCOPE HANDLE is a medical device that received FDA 510(k) clearance on 1989-10-30. The listed applicant is Michigan Instruments, Inc.. The 510(k) number is K895954.

When did LARYNGOSTAT LARYNGOSCOPE HANDLE receive FDA 510(k) clearance?

LARYNGOSTAT LARYNGOSCOPE HANDLE received FDA 510(k) clearance on 1989-10-30, under 510(k) number K895954.

Who is the listed applicant for LARYNGOSTAT LARYNGOSCOPE HANDLE?

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

What is the FDA product code for LARYNGOSTAT LARYNGOSCOPE HANDLE?

The FDA product code for LARYNGOSTAT LARYNGOSCOPE HANDLE is CCW.

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Other records listing Michigan Instruments, 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.

K073079THUMPER, MODEL: 1008K972525THUMPERK962237THUMPER CARDIOPULMONARY RESUSCITATORK851139THUMPER CARDIOPULMONARY RESUSCITATOR 1005K833879CARDIOPULMONARY RESUSCITATORK811909CARDIOPULMUNARY RESUSCITATOR

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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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