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FDA 510(k)

FERRIS BONE MARROW -NEEDLE-(DISPOSABLE)

K-Number: K800407 · 1980-03-12

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

Device Summary

FERRIS BONE MARROW -NEEDLE-(DISPOSABLE) 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 K800407. 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 FERRIS BONE MARROW -NEEDLE-(DISPOSABLE)?

FERRIS BONE MARROW -NEEDLE-(DISPOSABLE) 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 K800407.

When did FERRIS BONE MARROW -NEEDLE-(DISPOSABLE) receive FDA 510(k) clearance?

FERRIS BONE MARROW -NEEDLE-(DISPOSABLE) received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800407.

Who is the listed applicant for FERRIS BONE MARROW -NEEDLE-(DISPOSABLE)?

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 -NEEDLE-(DISPOSABLE)?

The FDA product code for FERRIS BONE MARROW -NEEDLE-(DISPOSABLE) 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. 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: 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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