Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206

K-Number: K002444 · 2000-10-18

Decision Date2000-10-18
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206 is the device name listed in this FDA 510(k) record. The listed applicant is Sun Nuclear Corp.. It received FDA 510(k) clearance on 2000-10-18 under 510(k) number K002444. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206?

PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206 is a medical device that received FDA 510(k) clearance on 2000-10-18. The listed applicant is Sun Nuclear Corp.. The 510(k) number is K002444.

When did PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206 receive FDA 510(k) clearance?

PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206 received FDA 510(k) clearance on 2000-10-18, under 510(k) number K002444.

Who is the listed applicant for PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206?

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

What is the FDA product code for PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206?

The FDA product code for PRECISION DOSIMETRY ELECTROMETER, MODEL 1010 OR 206 is IYE.

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 Sun Nuclear 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.

View all 13 devices →

Related Devices (Code: IYE)

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.

↑