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FDA 510(k)

CORNING 102 PRINTER

K-Number: K830296 · 1983-03-25

ApplicantCorning Medical & Scientific
Decision Date1983-03-25
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORNING 102 PRINTER 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 1983-03-25 under 510(k) number K830296. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNING 102 PRINTER?

CORNING 102 PRINTER is a medical device that received FDA 510(k) clearance on 1983-03-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K830296.

When did CORNING 102 PRINTER receive FDA 510(k) clearance?

CORNING 102 PRINTER received FDA 510(k) clearance on 1983-03-25, under 510(k) number K830296.

Who is the listed applicant for CORNING 102 PRINTER?

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 102 PRINTER?

The FDA product code for CORNING 102 PRINTER is JQP.

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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: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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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