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FDA 510(k)

ST AIA-PACK CA 19-9

K-Number: K023240 · 2002-12-23

ApplicantTosoh Corp.
Decision Date2002-12-23
Product CodeNIG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ST AIA-PACK CA 19-9 is the device name listed in this FDA 510(k) record. The listed applicant is Tosoh Corp.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K023240. The device is classified under product code NIG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ST AIA-PACK CA 19-9?

ST AIA-PACK CA 19-9 is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Tosoh Corp.. The 510(k) number is K023240.

When did ST AIA-PACK CA 19-9 receive FDA 510(k) clearance?

ST AIA-PACK CA 19-9 received FDA 510(k) clearance on 2002-12-23, under 510(k) number K023240.

Who is the listed applicant for ST AIA-PACK CA 19-9?

The FDA 510(k) record lists Tosoh Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ST AIA-PACK CA 19-9?

The FDA product code for ST AIA-PACK CA 19-9 is NIG.

Other records listing Tosoh Corp. 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.

K023239AIA-PACK CA 19-9K923021AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEMK913663AIA-PACK T-UK913298AIA-PACK CK-MBK913493AIA-PACK FT4K903628AIA-PACK IRI

View all 11 devices →

Related Devices (Code: NIG)

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.

K253528Atellica IM CA 19-9 IISiemens Healthcare Diagnostics, Inc.K231525VITROS Immunodiagnostic Products CA 19-9TM Reagent PackOrtho Clinical DiagnosticsK200997Lumipulse G CA19-9-NFujirebio Diagnostics,Inc.K191973Lumpipulse G CA19-9-NFujirebio Dianostics, Inc.K100375DIMENSION VISTA LOCI CA 19-9 FLEX REAGENT CARTRIDGE, AND DIMENSION LOCI7 CALIBRATOR WITH MODEL(S) K6457, AND KC604Siemens Healthcare Diagnostics, Inc.K052889VITROS CA 19-9Fujirebio Diagnostics,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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