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FDA 510(k)

ADMS BIOPSY NEEDLE

K-Number: K890203 · 1989-03-08

ApplicantAdvanced Diagnostic Medical Systems, Inc.
Decision Date1989-03-08
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADMS BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. It received FDA 510(k) clearance on 1989-03-08 under 510(k) number K890203. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADMS BIOPSY NEEDLE?

ADMS BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1989-03-08. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. The 510(k) number is K890203.

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

ADMS BIOPSY NEEDLE received FDA 510(k) clearance on 1989-03-08, under 510(k) number K890203.

Who is the listed applicant for ADMS BIOPSY NEEDLE?

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

What is the FDA product code for ADMS BIOPSY NEEDLE?

The FDA product code for ADMS BIOPSY NEEDLE is FCG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Advanced Diagnostic Medical Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K882746ADMS SILENT NEEDLE GUNK881208PROBE SHEATH FOR ADMS ULTRASOUND PROBEK875119BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE

Related Devices (Code: FCG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252646Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)Olympus Medical Systems Corp.K250994ClearTip FNA and FNB TypesFinemedix Co., Ltd.K241209EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19)Cook Ireland, Ltd.K231422Precision GILimaca Medical, Ltd.K231267ClearTipFinemedix Co., Ltd.K230909EchoTip® AcuCore™ Ultrasound Biopsy Needle (ECHO-BX-3-22)Cook Ireland, Ltd.

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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