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FDA 510(k)

TUMORLOCALIZER MRI

K-Number: K962615 · 1998-03-19

ApplicantFerguson Medical
Decision Date1998-03-19
Product CodeMIG
DecisionSubstantially Equivalent

Device Summary

TUMORLOCALIZER MRI is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1998-03-19 under 510(k) number K962615. The device is classified under product code MIG. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUMORLOCALIZER MRI?

TUMORLOCALIZER MRI is a medical device that received FDA 510(k) clearance on 1998-03-19. The listed applicant is Ferguson Medical. The 510(k) number is K962615.

When did TUMORLOCALIZER MRI receive FDA 510(k) clearance?

TUMORLOCALIZER MRI received FDA 510(k) clearance on 1998-03-19, under 510(k) number K962615.

Who is the listed applicant for TUMORLOCALIZER MRI?

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

What is the FDA product code for TUMORLOCALIZER MRI?

The FDA product code for TUMORLOCALIZER MRI is MIG.

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Other records listing Ferguson Medical 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.

K033153DICOM THEATERK963794PUNCTURENEEDLEK971813EMBLAK972217ORTHOPEDIC SCREW SYSTEMK972219ORTHOPEDIC PLATE SYSTEMK970819TARGOBEAM

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Related Devices (Code: MIG)

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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