FDA 510(k)

LIGHT SABER CORE TISSUE NEEDLE

K-Number: K981796 · 1998-08-05

Decision Date1998-08-05

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

LIGHT SABER CORE TISSUE NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Minrad, Inc.. It received FDA 510(k) clearance on 1998-08-05 under 510(k) number K981796. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT SABER CORE TISSUE NEEDLE?

LIGHT SABER CORE TISSUE NEEDLE is a medical device that received FDA 510(k) clearance on 1998-08-05. The listed applicant is Minrad, Inc.. The 510(k) number is K981796.

When did LIGHT SABER CORE TISSUE NEEDLE receive FDA 510(k) clearance?

LIGHT SABER CORE TISSUE NEEDLE received FDA 510(k) clearance on 1998-08-05, under 510(k) number K981796.

Who is the listed applicant for LIGHT SABER CORE TISSUE NEEDLE?

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

What is the FDA product code for LIGHT SABER CORE TISSUE NEEDLE?

The FDA product code for LIGHT SABER CORE TISSUE NEEDLE is KNW.

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Other records listing Minrad, Inc. as applicant

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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.