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FDA 510(k)

MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM

K-Number: K940660 · 1994-12-09

ApplicantVictoreen, Inc.
Decision Date1994-12-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1994-12-09 under 510(k) number K940660. 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 MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM?

MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1994-12-09. The listed applicant is Victoreen, Inc.. The 510(k) number is K940660.

When did MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM receive FDA 510(k) clearance?

MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM received FDA 510(k) clearance on 1994-12-09, under 510(k) number K940660.

Who is the listed applicant for MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM?

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

What is the FDA product code for MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM?

The FDA product code for MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM is IYE.

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Other records listing Victoreen, 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.

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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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