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FDA 510(k)

DISPOSABLE ENT PUNCH

K-Number: K942065 · 1994-06-06

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1994-06-06
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ENT PUNCH 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 1994-06-06 under 510(k) number K942065. 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 ENT PUNCH?

DISPOSABLE ENT PUNCH is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K942065.

When did DISPOSABLE ENT PUNCH receive FDA 510(k) clearance?

DISPOSABLE ENT PUNCH received FDA 510(k) clearance on 1994-06-06, under 510(k) number K942065.

Who is the listed applicant for DISPOSABLE ENT PUNCH?

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 ENT PUNCH?

The FDA product code for DISPOSABLE ENT PUNCH is LRC.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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