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FDA 510(k)

TOSOH AIA-PACK T3

K-Number: K897001 · 1990-03-09

ApplicantTosoh Corp.
Decision Date1990-03-09
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOSOH AIA-PACK T3 is the device name listed in this FDA 510(k) record. The listed applicant is Tosoh Corp.. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K897001. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOSOH AIA-PACK T3?

TOSOH AIA-PACK T3 is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Tosoh Corp.. The 510(k) number is K897001.

When did TOSOH AIA-PACK T3 receive FDA 510(k) clearance?

TOSOH AIA-PACK T3 received FDA 510(k) clearance on 1990-03-09, under 510(k) number K897001.

Who is the listed applicant for TOSOH AIA-PACK T3?

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 TOSOH AIA-PACK T3?

The FDA product code for TOSOH AIA-PACK T3 is CDP.

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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 19-9K023240ST AIA-PACK CA 19-9K923021AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEMK913663AIA-PACK T-UK913298AIA-PACK CK-MBK913493AIA-PACK FT4

View all 11 devices →

Related Devices (Code: CDP)

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.

K001607REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)Repromedix Corp.K991692CHIRON DIAGNOSTICS ACS: 180 FT3Chiron Diagnostics Corp.K991311TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005Biocheck, Inc.K991252AIA-PACK FT3 ASSAYTosoh Medics, Inc.K981824OPTICOAT T3 EIA KITBiotecx Laboratories, Inc.K983439ABBOTT ARCHITECT FREE T3Abbott Laboratories

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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