FDA 510(k)

STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE

K-Number: K885169 · 1989-02-27

Decision Date1989-02-27

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1989-02-27 under 510(k) number K885169. 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 STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE?

STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1989-02-27. The listed applicant is Boston Scientific Corp. The 510(k) number is K885169.

When did STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE receive FDA 510(k) clearance?

STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE received FDA 510(k) clearance on 1989-02-27, under 510(k) number K885169.

Who is the listed applicant for STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE?

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

What is the FDA product code for STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE?

The FDA product code for STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE is KNW.

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Other records listing Boston Scientific Corp as applicant

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Related Devices (Code: 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.