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FDA 510(k)

FLAME PHOTOMETER MODEL 460

K-Number: K771303 · 1977-08-22

ApplicantCorning Medical & Scientific
Decision Date1977-08-22
Product CodeJIH
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

FLAME PHOTOMETER MODEL 460 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 1977-08-22 under 510(k) number K771303. The device is classified under product code JIH. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLAME PHOTOMETER MODEL 460?

FLAME PHOTOMETER MODEL 460 is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Corning Medical & Scientific. The 510(k) number is K771303.

When did FLAME PHOTOMETER MODEL 460 receive FDA 510(k) clearance?

FLAME PHOTOMETER MODEL 460 received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771303.

Who is the listed applicant for FLAME PHOTOMETER MODEL 460?

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 FLAME PHOTOMETER MODEL 460?

The FDA product code for FLAME PHOTOMETER MODEL 460 is JIH.

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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: JIH)

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.

K050338MODIFICATION TO: INSTAREAD LITHIUM SYSTEMAkers Biosciences, Inc.K031579INSTAREAD LITHIUM SYSTEMAkers Laboratories, Inc.K011033DIMENSION LITHIUM (LI) FLEX REAGENT CARTRIDGE, MODEL DF 132Dade Behring, Inc.K934106KODAK EKTACHEM DTSC II SLIDES (LI)Eastman Kodak CompanyK924488KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (LI)Eastman Kodak CompanyK921403MODEL 654 ANALYZERCiba Corning Diagnostics Corp.

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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