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FDA 510(k)

XPS STRAIGHTSHOT MICRORESECTOR

K-Number: K972453 · 1997-09-05

ApplicantXomed, Inc.
Decision Date1997-09-05
Product CodeERL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

XPS STRAIGHTSHOT MICRORESECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1997-09-05 under 510(k) number K972453. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XPS STRAIGHTSHOT MICRORESECTOR?

XPS STRAIGHTSHOT MICRORESECTOR is a medical device that received FDA 510(k) clearance on 1997-09-05. The listed applicant is Xomed, Inc.. The 510(k) number is K972453.

When did XPS STRAIGHTSHOT MICRORESECTOR receive FDA 510(k) clearance?

XPS STRAIGHTSHOT MICRORESECTOR received FDA 510(k) clearance on 1997-09-05, under 510(k) number K972453.

Who is the listed applicant for XPS STRAIGHTSHOT MICRORESECTOR?

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 XPS STRAIGHTSHOT MICRORESECTOR?

The FDA product code for XPS STRAIGHTSHOT MICRORESECTOR is ERL.

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: ERL)

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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