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FDA 510(k)

ADT PERITONEAL LAVAGE TRAY (DISP.)

K-Number: K800421 · 1980-03-25

ApplicantA.D.T. Lab Industries
Decision Date1980-03-25
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADT PERITONEAL LAVAGE TRAY (DISP.) 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 K800421. 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 ADT PERITONEAL LAVAGE TRAY (DISP.)?

ADT PERITONEAL LAVAGE TRAY (DISP.) 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 K800421.

When did ADT PERITONEAL LAVAGE TRAY (DISP.) receive FDA 510(k) clearance?

ADT PERITONEAL LAVAGE TRAY (DISP.) received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800421.

Who is the listed applicant for ADT PERITONEAL LAVAGE TRAY (DISP.)?

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 PERITONEAL LAVAGE TRAY (DISP.)?

The FDA product code for ADT PERITONEAL LAVAGE TRAY (DISP.) 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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