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FDA 510(k)

ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL

K-Number: K800417 · 1980-04-28

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

Device Summary

ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL 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 K800417. 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 PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL?

ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL 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 K800417.

When did ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL receive FDA 510(k) clearance?

ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL received FDA 510(k) clearance on 1980-04-28, under 510(k) number K800417.

Who is the listed applicant for ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL?

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 PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL?

The FDA product code for ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL 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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