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FDA 510(k)

ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL

K-Number: K800419 · 1980-03-25

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

Device Summary

ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL 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 K800419. 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 TRANSHEPATIC DISP. CHOL?

ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL 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 K800419.

When did ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL receive FDA 510(k) clearance?

ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800419.

Who is the listed applicant for ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL?

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 TRANSHEPATIC DISP. CHOL?

The FDA product code for ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL 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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