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FDA 510(k)

FIBEROPTIC LARYNGOSCOPE HANDLE

K-Number: K944686 · 1994-11-04

ApplicantFiberoptic Medical Products, Inc.
Decision Date1994-11-04
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FIBEROPTIC LARYNGOSCOPE HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Fiberoptic Medical Products, Inc.. It received FDA 510(k) clearance on 1994-11-04 under 510(k) number K944686. 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 FIBEROPTIC LARYNGOSCOPE HANDLE?

FIBEROPTIC LARYNGOSCOPE HANDLE is a medical device that received FDA 510(k) clearance on 1994-11-04. The listed applicant is Fiberoptic Medical Products, Inc.. The 510(k) number is K944686.

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

FIBEROPTIC LARYNGOSCOPE HANDLE received FDA 510(k) clearance on 1994-11-04, under 510(k) number K944686.

Who is the listed applicant for FIBEROPTIC LARYNGOSCOPE HANDLE?

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

What is the FDA product code for FIBEROPTIC LARYNGOSCOPE HANDLE?

The FDA product code for FIBEROPTIC LARYNGOSCOPE HANDLE 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 Fiberoptic Medical Products, 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.

K933598ENDOSTAR(TM) STYLETK921393IMAGICA MICRO-ENDOSCOPEK912252INFINITY(R) TRANSILLUMINATOR EXAMINATION LIGHTK883779WALLABY(TM) BLANKET

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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