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FDA 510(k)

MRTOFLM COMPUTER PROGRAM

K-Number: K960293 · 1996-08-01

ApplicantNorthwest Medical Physics Equipment, Inc.
Decision Date1996-08-01
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRTOFLM COMPUTER PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Northwest Medical Physics Equipment, Inc.. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K960293. 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 MRTOFLM COMPUTER PROGRAM?

MRTOFLM COMPUTER PROGRAM is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Northwest Medical Physics Equipment, Inc.. The 510(k) number is K960293.

When did MRTOFLM COMPUTER PROGRAM receive FDA 510(k) clearance?

MRTOFLM COMPUTER PROGRAM received FDA 510(k) clearance on 1996-08-01, under 510(k) number K960293.

Who is the listed applicant for MRTOFLM COMPUTER PROGRAM?

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

What is the FDA product code for MRTOFLM COMPUTER PROGRAM?

The FDA product code for MRTOFLM COMPUTER 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.

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Other records listing Northwest Medical Physics Equipment, 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.

K063274ACCULOC BREAST LOCALIZATION SYSTEMK012575PREFERNCE IMRT TREATMENT PLANNING MODULEK001833PREFERENCE TREATMENT SYSTEMK983793PREFERENCE TREATMENT SYSTEMK970464P REFERENCE TPS (TREATMENT PLANNING SOFTWARE) 1.1

Related Devices (Code: IYE)

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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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