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FDA 510(k)

RIA KIT, IMMO PHASE

K-Number: K781953 · 1979-02-01

ApplicantCorning Medical & Scientific
Decision Date1979-02-01
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, IMMO PHASE 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 1979-02-01 under 510(k) number K781953. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA KIT, IMMO PHASE?

RIA KIT, IMMO PHASE is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Corning Medical & Scientific. The 510(k) number is K781953.

When did RIA KIT, IMMO PHASE receive FDA 510(k) clearance?

RIA KIT, IMMO PHASE received FDA 510(k) clearance on 1979-02-01, under 510(k) number K781953.

Who is the listed applicant for RIA KIT, IMMO PHASE?

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 RIA KIT, IMMO PHASE?

The FDA product code for RIA KIT, IMMO PHASE is JLW.

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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: JLW)

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.

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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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