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FDA 510(k)

MUCHECK MONITOR UNIT VALIDATION PROGRAM

K-Number: K980904 · 1998-06-08

Decision Date1998-06-08
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MUCHECK MONITOR UNIT VALIDATION PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dosimetry Services, Inc.. It received FDA 510(k) clearance on 1998-06-08 under 510(k) number K980904. 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 MUCHECK MONITOR UNIT VALIDATION PROGRAM?

MUCHECK MONITOR UNIT VALIDATION PROGRAM is a medical device that received FDA 510(k) clearance on 1998-06-08. The listed applicant is Medical Dosimetry Services, Inc.. The 510(k) number is K980904.

When did MUCHECK MONITOR UNIT VALIDATION PROGRAM receive FDA 510(k) clearance?

MUCHECK MONITOR UNIT VALIDATION PROGRAM received FDA 510(k) clearance on 1998-06-08, under 510(k) number K980904.

Who is the listed applicant for MUCHECK MONITOR UNIT VALIDATION PROGRAM?

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

What is the FDA product code for MUCHECK MONITOR UNIT VALIDATION PROGRAM?

The FDA product code for MUCHECK MONITOR UNIT VALIDATION PROGRAM 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.

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

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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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