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FDA 510(k)

DATA TERMINAL MODEL 722

K-Number: K781217 · 1978-08-21

Decision Date1978-08-21
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DATA TERMINAL MODEL 722 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 1978-08-21 under 510(k) number K781217. 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 DATA TERMINAL MODEL 722?

DATA TERMINAL MODEL 722 is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Corning Medical & Scientific. The 510(k) number is K781217.

When did DATA TERMINAL MODEL 722 receive FDA 510(k) clearance?

DATA TERMINAL MODEL 722 received FDA 510(k) clearance on 1978-08-21, under 510(k) number K781217.

Who is the listed applicant for DATA TERMINAL MODEL 722?

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 DATA TERMINAL MODEL 722?

The FDA product code for DATA TERMINAL MODEL 722 is JQP.

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: 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.

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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