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FDA 510(k)

MODIFIED VERSAPORT

K-Number: K954108 · 1995-10-17

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1995-10-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED VERSAPORT 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 1995-10-17 under 510(k) number K954108. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED VERSAPORT?

MODIFIED VERSAPORT is a medical device that received FDA 510(k) clearance on 1995-10-17. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K954108.

When did MODIFIED VERSAPORT receive FDA 510(k) clearance?

MODIFIED VERSAPORT received FDA 510(k) clearance on 1995-10-17, under 510(k) number K954108.

Who is the listed applicant for MODIFIED VERSAPORT?

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 MODIFIED VERSAPORT?

The FDA product code for MODIFIED VERSAPORT is GCJ.

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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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