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FDA 510(k)

ADT DISPOSABLE THIN NEEDLE ASPIRATION

K-Number: K800418 · 1980-04-28

ApplicantA.D.T. Lab Industries
Decision Date1980-04-28
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADT DISPOSABLE THIN NEEDLE ASPIRATION 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 1980-04-28 under 510(k) number K800418. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADT DISPOSABLE THIN NEEDLE ASPIRATION?

ADT DISPOSABLE THIN NEEDLE ASPIRATION is a medical device that received FDA 510(k) clearance on 1980-04-28. The listed applicant is A.D.T. Lab Industries. The 510(k) number is K800418.

When did ADT DISPOSABLE THIN NEEDLE ASPIRATION receive FDA 510(k) clearance?

ADT DISPOSABLE THIN NEEDLE ASPIRATION received FDA 510(k) clearance on 1980-04-28, under 510(k) number K800418.

Who is the listed applicant for ADT DISPOSABLE THIN NEEDLE ASPIRATION?

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 DISPOSABLE THIN NEEDLE ASPIRATION?

The FDA product code for ADT DISPOSABLE THIN NEEDLE ASPIRATION is FSM.

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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: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.

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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