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FDA 510(k)

MODIFIED CHERNE CAD DETECTOR

K-Number: K860015 · 1986-04-23

ApplicantCherne Industries, Inc.
Decision Date1986-04-23
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED CHERNE CAD DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cherne Industries, Inc.. It received FDA 510(k) clearance on 1986-04-23 under 510(k) number K860015. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CHERNE CAD DETECTOR?

MODIFIED CHERNE CAD DETECTOR is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Cherne Industries, Inc.. The 510(k) number is K860015.

When did MODIFIED CHERNE CAD DETECTOR receive FDA 510(k) clearance?

MODIFIED CHERNE CAD DETECTOR received FDA 510(k) clearance on 1986-04-23, under 510(k) number K860015.

Who is the listed applicant for MODIFIED CHERNE CAD DETECTOR?

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

What is the FDA product code for MODIFIED CHERNE CAD DETECTOR?

The FDA product code for MODIFIED CHERNE CAD DETECTOR is DXG.

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.

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Other records listing Cherne Industries, 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.

K864072ADEC 1005-C CHAIRK852900CVERNE CAD DETECTOR

Related Devices (Code: DXG)

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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