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FDA 510(k)

AUTO-CON

K-Number: K781007 · 1978-06-30

Decision Date1978-06-30
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

AUTO-CON is the device name listed in this FDA 510(k) record. The listed applicant is Barnes-Hind, Inc.. It received FDA 510(k) clearance on 1978-06-30 under 510(k) number K781007. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-CON?

AUTO-CON is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Barnes-Hind, Inc.. The 510(k) number is K781007.

When did AUTO-CON receive FDA 510(k) clearance?

AUTO-CON received FDA 510(k) clearance on 1978-06-30, under 510(k) number K781007.

Who is the listed applicant for AUTO-CON?

The FDA 510(k) record lists Barnes-Hind, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO-CON?

The FDA product code for AUTO-CON is HPX.

Other records listing Barnes-Hind, Inc. 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 7 devices →

Related Devices (Code: HPX)

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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