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FDA 510(k)

XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT

K-Number: K983025 · 1998-11-06

ApplicantXomed, Inc.
Decision Date1998-11-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1998-11-06 under 510(k) number K983025. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT?

XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT is a medical device that received FDA 510(k) clearance on 1998-11-06. The listed applicant is Xomed, Inc.. The 510(k) number is K983025.

When did XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT receive FDA 510(k) clearance?

XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT received FDA 510(k) clearance on 1998-11-06, under 510(k) number K983025.

Who is the listed applicant for XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT?

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

What is the FDA product code for XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT?

The FDA product code for XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT is HRX.

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 Xomed, 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 82 devices →

Related Devices (Code: HRX)

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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