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FDA 510(k)

DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM

K-Number: K083035 · 2008-11-13

Decision Date2008-11-13
Product CodeNZT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sicel Technologies, Inc.. It received FDA 510(k) clearance on 2008-11-13 under 510(k) number K083035. The device is classified under product code NZT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM?

DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-11-13. The listed applicant is Sicel Technologies, Inc.. The 510(k) number is K083035.

When did DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM receive FDA 510(k) clearance?

DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM received FDA 510(k) clearance on 2008-11-13, under 510(k) number K083035.

Who is the listed applicant for DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM?

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

What is the FDA product code for DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM?

The FDA product code for DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM is NZT.

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 Sicel Technologies, 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.

View all 7 devices →

Related Devices (Code: NZT)

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

View on FDA Database →

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

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