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FDA 510(k)

ELA MEDICAL ANATEC HOLTER SCANNER

K-Number: K792239 · 1979-11-07

Decision Date1979-11-07
Product Code
DecisionUnknown

Device Summary

ELA MEDICAL ANATEC HOLTER SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Ela Medical, Inc.. It received FDA 510(k) clearance on 1979-11-07 under 510(k) number K792239. FDA Decision: Unknown.

Frequently Asked Questions

What is the ELA MEDICAL ANATEC HOLTER SCANNER?

ELA MEDICAL ANATEC HOLTER SCANNER is a medical device that received FDA 510(k) clearance on 1979-11-07. The listed applicant is Ela Medical, Inc.. The 510(k) number is K792239.

When did ELA MEDICAL ANATEC HOLTER SCANNER receive FDA 510(k) clearance?

ELA MEDICAL ANATEC HOLTER SCANNER received FDA 510(k) clearance on 1979-11-07, under 510(k) number K792239.

Who is the listed applicant for ELA MEDICAL ANATEC HOLTER SCANNER?

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

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 Ela Medical, 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.

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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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