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FDA 510(k)

ULTRACLIP TISSUE MARKER

K-Number: K993785 · 2000-02-04

ApplicantInrad
Decision Date2000-02-04
Product CodeGDW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRACLIP TISSUE MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Inrad. It received FDA 510(k) clearance on 2000-02-04 under 510(k) number K993785. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACLIP TISSUE MARKER?

ULTRACLIP TISSUE MARKER is a medical device that received FDA 510(k) clearance on 2000-02-04. The listed applicant is Inrad. The 510(k) number is K993785.

When did ULTRACLIP TISSUE MARKER receive FDA 510(k) clearance?

ULTRACLIP TISSUE MARKER received FDA 510(k) clearance on 2000-02-04, under 510(k) number K993785.

Who is the listed applicant for ULTRACLIP TISSUE MARKER?

The FDA 510(k) record lists Inrad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRACLIP TISSUE MARKER?

The FDA product code for ULTRACLIP TISSUE MARKER is GDW.

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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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