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FDA 510(k)

CORNING CERTAIN TM

K-Number: K820873 · 1982-04-16

Decision Date1982-04-16
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORNING CERTAIN TM 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 1982-04-16 under 510(k) number K820873. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNING CERTAIN TM?

CORNING CERTAIN TM is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Corning Medical & Scientific. The 510(k) number is K820873.

When did CORNING CERTAIN TM receive FDA 510(k) clearance?

CORNING CERTAIN TM received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820873.

Who is the listed applicant for CORNING CERTAIN TM?

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 CERTAIN TM?

The FDA product code for CORNING CERTAIN TM is JJS.

Related Clinical Trials

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.

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.

View all 111 devices →

Related Devices (Code: JJS)

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.

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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