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FDA 510(k)

MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002

K-Number: K041852 · 2004-11-15

ApplicantMinrad, Inc.
Decision Date2004-11-15
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 is the device name listed in this FDA 510(k) record. The listed applicant is Minrad, Inc.. It received FDA 510(k) clearance on 2004-11-15 under 510(k) number K041852. 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 MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?

MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 is a medical device that received FDA 510(k) clearance on 2004-11-15. The listed applicant is Minrad, Inc.. The 510(k) number is K041852.

When did MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 receive FDA 510(k) clearance?

MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 received FDA 510(k) clearance on 2004-11-15, under 510(k) number K041852.

Who is the listed applicant for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?

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

What is the FDA product code for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?

The FDA product code for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 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 Minrad, 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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