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FDA 510(k)

MICROMEDICS NASAL SEPTAL BUTTON

K-Number: K982667 · 1998-11-24

Decision Date1998-11-24
Product CodeLFB
DecisionSubstantially Equivalent

Device Summary

MICROMEDICS NASAL SEPTAL BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 1998-11-24 under 510(k) number K982667. The device is classified under product code LFB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMEDICS NASAL SEPTAL BUTTON?

MICROMEDICS NASAL SEPTAL BUTTON is a medical device that received FDA 510(k) clearance on 1998-11-24. The listed applicant is Micromedics, Inc.. The 510(k) number is K982667.

When did MICROMEDICS NASAL SEPTAL BUTTON receive FDA 510(k) clearance?

MICROMEDICS NASAL SEPTAL BUTTON received FDA 510(k) clearance on 1998-11-24, under 510(k) number K982667.

Who is the listed applicant for MICROMEDICS NASAL SEPTAL BUTTON?

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

What is the FDA product code for MICROMEDICS NASAL SEPTAL BUTTON?

The FDA product code for MICROMEDICS NASAL SEPTAL BUTTON is LFB.

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 Micromedics, 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.

View all 29 devices →

Related Devices (Code: LFB)

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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