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FDA 510(k)

DOSIMETRIC RELEASE OF RADIATION DEV

K-Number: K830327 · 1983-03-24

Decision Date1983-03-24
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOSIMETRIC RELEASE OF RADIATION DEV is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830327. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSIMETRIC RELEASE OF RADIATION DEV?

DOSIMETRIC RELEASE OF RADIATION DEV is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is American Bentley. The 510(k) number is K830327.

When did DOSIMETRIC RELEASE OF RADIATION DEV receive FDA 510(k) clearance?

DOSIMETRIC RELEASE OF RADIATION DEV received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830327.

Who is the listed applicant for DOSIMETRIC RELEASE OF RADIATION DEV?

The FDA 510(k) record lists American Bentley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOSIMETRIC RELEASE OF RADIATION DEV?

The FDA product code for DOSIMETRIC RELEASE OF RADIATION DEV is DTZ.

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 American Bentley 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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Related Devices (Code: DTZ)

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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