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FDA 510(k)

DISPOSABLE NASAL SCISSOR

K-Number: K942063 · 1994-06-08

Decision Date1994-06-08
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NASAL SCISSOR is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1994-06-08 under 510(k) number K942063. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE NASAL SCISSOR?

DISPOSABLE NASAL SCISSOR is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K942063.

When did DISPOSABLE NASAL SCISSOR receive FDA 510(k) clearance?

DISPOSABLE NASAL SCISSOR received FDA 510(k) clearance on 1994-06-08, under 510(k) number K942063.

Who is the listed applicant for DISPOSABLE NASAL SCISSOR?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE NASAL SCISSOR?

The FDA product code for DISPOSABLE NASAL SCISSOR is LRC.

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 United States Surgical, A Division of Tyco Healthc 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 218 devices →

Related Devices (Code: LRC)

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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