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FDA 510(k)

ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW

K-Number: K800412 · 1980-04-28

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

Device Summary

ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW 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 K800412. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW?

ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW 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 K800412.

When did ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW receive FDA 510(k) clearance?

ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW received FDA 510(k) clearance on 1980-04-28, under 510(k) number K800412.

Who is the listed applicant for ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW?

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 ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW?

The FDA product code for ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW is GAA.

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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. NEELDEK800414ADT SOFT TISSUE BIOPSY TRAYK800410ADT BONE MARROW BIOPSY-ASPIRATION TRAYK800408ADT BONE MAR. BIO/ASP. TRAY W/NEEDLE

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Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, 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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