FDA 510(k)

T19S BIOPSY NEEDLE

K-Number: K902077 · 1990-07-27

ApplicantOhio Medical Instrument Co., Inc.

Decision Date1990-07-27

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

T19S BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Instrument Co., Inc.. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K902077. 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 T19S BIOPSY NEEDLE?

T19S BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Ohio Medical Instrument Co., Inc.. The 510(k) number is K902077.

When did T19S BIOPSY NEEDLE receive FDA 510(k) clearance?

T19S BIOPSY NEEDLE received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902077.

Who is the listed applicant for T19S BIOPSY NEEDLE?

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

What is the FDA product code for T19S BIOPSY NEEDLE?

The FDA product code for T19S BIOPSY NEEDLE is KNW.

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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.