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FDA 510(k)

NON-FERMENTER SYSTEM

K-Number: K772112 · 1977-11-17

ApplicantCorning Medical & Scientific
Decision Date1977-11-17
Product CodeJSW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NON-FERMENTER SYSTEM 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 1977-11-17 under 510(k) number K772112. The device is classified under product code JSW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-FERMENTER SYSTEM?

NON-FERMENTER SYSTEM is a medical device that received FDA 510(k) clearance on 1977-11-17. The listed applicant is Corning Medical & Scientific. The 510(k) number is K772112.

When did NON-FERMENTER SYSTEM receive FDA 510(k) clearance?

NON-FERMENTER SYSTEM received FDA 510(k) clearance on 1977-11-17, under 510(k) number K772112.

Who is the listed applicant for NON-FERMENTER SYSTEM?

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 NON-FERMENTER SYSTEM?

The FDA product code for NON-FERMENTER SYSTEM is JSW.

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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

View all 111 devices →

Related Devices (Code: JSW)

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.

K922768RAPID NFT, MODIFICATIONBiomerieux Vitek, Inc.K900517RAPID NF SYSTEMInnovative Diagnostic Systems, Inc.K870769AUSTIN NONFERMENTER KITAustin Biological LaboratoriesK790992PSEUDO-PALETTE TMMicro-Palettes, Inc.K770745PANEL, GNF, MICRO-IDMicro-Media Systems, 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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