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FDA 510(k)

AUTONOM

K-Number: K780312 · 1978-04-05

Decision Date1978-04-05
Product CodeKNM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AUTONOM is the device name listed in this FDA 510(k) record. The listed applicant is Autonomic Equipment Supply Co,. It received FDA 510(k) clearance on 1978-04-05 under 510(k) number K780312. The device is classified under product code KNM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTONOM?

AUTONOM is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is Autonomic Equipment Supply Co,. The 510(k) number is K780312.

When did AUTONOM receive FDA 510(k) clearance?

AUTONOM received FDA 510(k) clearance on 1978-04-05, under 510(k) number K780312.

Who is the listed applicant for AUTONOM?

The FDA 510(k) record lists Autonomic Equipment Supply Co, as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTONOM?

The FDA product code for AUTONOM is KNM.

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.

Related PubMed Literature

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 Autonomic Equipment Supply Co, 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.

Related Devices (Code: KNM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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