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FDA 510(k)

NOSEBLEED NOSECLIP

K-Number: K981966 · 1998-08-14

ApplicantMichael M. Knott, M.D.
Decision Date1998-08-14
Product CodeEMX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NOSEBLEED NOSECLIP is the device name listed in this FDA 510(k) record. The listed applicant is Michael M. Knott, M.D.. It received FDA 510(k) clearance on 1998-08-14 under 510(k) number K981966. The device is classified under product code EMX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOSEBLEED NOSECLIP?

NOSEBLEED NOSECLIP is a medical device that received FDA 510(k) clearance on 1998-08-14. The listed applicant is Michael M. Knott, M.D.. The 510(k) number is K981966.

When did NOSEBLEED NOSECLIP receive FDA 510(k) clearance?

NOSEBLEED NOSECLIP received FDA 510(k) clearance on 1998-08-14, under 510(k) number K981966.

Who is the listed applicant for NOSEBLEED NOSECLIP?

The FDA 510(k) record lists Michael M. Knott, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOSEBLEED NOSECLIP?

The FDA product code for NOSEBLEED NOSECLIP is EMX.

Related Clinical Trials

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Other records listing Michael M. Knott, M.D. 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.

K971354KNOTT NG TUBE

Related Devices (Code: EMX)

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.

K220326PosiSep X BAM Hemostat Dressing/Intranasal SplintHemostasis, LLCK041446NASALCEASELes Laboratorires Brothier, S.A.K000108RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100Bhk HoldingK993362HYLASINEBiomatrix, Inc.K983276HYDROFERA BACTERISTATIC NASAL DRESSINGHydrofera, LLCK982731MEROGEL NASAL DRESSING AND SINUS STENTXomed, 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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