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FDA 510(k)

ADT PERCUTANEOUS NON-DISP. NEEDLE

K-Number: K800420 · 1980-03-25

ApplicantA.D.T. Lab Industries
Decision Date1980-03-25
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADT PERCUTANEOUS NON-DISP. NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is A.D.T. Lab Industries. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800420. 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 ADT PERCUTANEOUS NON-DISP. NEEDLE?

ADT PERCUTANEOUS NON-DISP. NEEDLE is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is A.D.T. Lab Industries. The 510(k) number is K800420.

When did ADT PERCUTANEOUS NON-DISP. NEEDLE receive FDA 510(k) clearance?

ADT PERCUTANEOUS NON-DISP. NEEDLE received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800420.

Who is the listed applicant for ADT PERCUTANEOUS NON-DISP. NEEDLE?

The FDA 510(k) record lists A.D.T. Lab Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADT PERCUTANEOUS NON-DISP. NEEDLE?

The FDA product code for ADT PERCUTANEOUS NON-DISP. NEEDLE is FCG.

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Other records listing A.D.T. Lab Industries 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.

K812297A.D.T. PROCEDURES TRAYK801754ADT BONE MARROW ASPIRATION NEEDLEK801753ADT BONE MARROW BIOPSY-ASPIR. NEELDEK800410ADT BONE MARROW BIOPSY-ASPIRATION TRAYK800408ADT BONE MAR. BIO/ASP. TRAY W/NEEDLEK800412ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW

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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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