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FDA 510(k)

CORNING IMMO PHASE FREE T3

K-Number: K840222 · 1984-05-07

ApplicantCorning Medical & Scientific
Decision Date1984-05-07
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORNING IMMO PHASE FREE T3 is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1984-05-07 under 510(k) number K840222. 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 CORNING IMMO PHASE FREE T3?

CORNING IMMO PHASE FREE T3 is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Corning Medical & Scientific. The 510(k) number is K840222.

When did CORNING IMMO PHASE FREE T3 receive FDA 510(k) clearance?

CORNING IMMO PHASE FREE T3 received FDA 510(k) clearance on 1984-05-07, under 510(k) number K840222.

Who is the listed applicant for CORNING IMMO PHASE FREE T3?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORNING IMMO PHASE FREE T3?

The FDA product code for CORNING IMMO PHASE FREE T3 is CDP.

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Other records listing Corning Medical & Scientific 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.

K875122DISPOSABLE STERILE SYRINGE FILTERSK872273CORNING EASY WASH ELISA PLATESK872076CORNING DISPOSABLE ROLLER BOTTLESK863789CORNING ELISA PLATESK854024CORNING MAGIC MAB HCG RADIOIMMUNOASSAYK853634CORNING CELL WELLS-MULTIPLE WELL PLATES

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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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