FDA 510(k)

DEXIDE BIPOLAR FORCEPS II ** DEVICE

K-Number: K991859 · 1999-06-23

ApplicantUnited States Surgical, A Division of Tyco Healthc

Decision Date1999-06-23

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DEXIDE BIPOLAR FORCEPS II ** DEVICE 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 1999-06-23 under 510(k) number K991859. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE BIPOLAR FORCEPS II ** DEVICE?

DEXIDE BIPOLAR FORCEPS II ** DEVICE is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K991859.

When did DEXIDE BIPOLAR FORCEPS II ** DEVICE receive FDA 510(k) clearance?

DEXIDE BIPOLAR FORCEPS II ** DEVICE received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991859.

Who is the listed applicant for DEXIDE BIPOLAR FORCEPS II ** DEVICE?

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 DEXIDE BIPOLAR FORCEPS II ** DEVICE?

The FDA product code for DEXIDE BIPOLAR FORCEPS II ** DEVICE is GEI.

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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.