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FDA 510(k)

NATURAL DETECTOR SYSTEM

K-Number: K861731 · 1986-11-06

Decision Date1986-11-06
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

NATURAL DETECTOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Health Resources Corp.. It received FDA 510(k) clearance on 1986-11-06 under 510(k) number K861731. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATURAL DETECTOR SYSTEM?

NATURAL DETECTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1986-11-06. The listed applicant is U.S. Health Resources Corp.. The 510(k) number is K861731.

When did NATURAL DETECTOR SYSTEM receive FDA 510(k) clearance?

NATURAL DETECTOR SYSTEM received FDA 510(k) clearance on 1986-11-06, under 510(k) number K861731.

Who is the listed applicant for NATURAL DETECTOR SYSTEM?

The FDA 510(k) record lists U.S. Health Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NATURAL DETECTOR SYSTEM?

The FDA product code for NATURAL DETECTOR SYSTEM is KHE.

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 U.S. Health Resources Corp. 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: KHE)

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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