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FDA 510(k)

FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE

K-Number: K800406 · 1980-03-12

ApplicantA.D.T. Lab Industries
Decision Date1980-03-12
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FERRIS BONE MARROW BIOPSY-ASPIR. 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 1980-03-12 under 510(k) number K800406. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE?

FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is A.D.T. Lab Industries. The 510(k) number is K800406.

When did FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE receive FDA 510(k) clearance?

FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800406.

Who is the listed applicant for FERRIS BONE MARROW BIOPSY-ASPIR. 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 FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE?

The FDA product code for FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE is GDM.

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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: GDM)

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.

K071732MARROWMINERStemcor Systems, Inc.K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.

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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