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FDA 510(k)

TARGOBEAM

K-Number: K970819 · 1997-07-14

ApplicantFerguson Medical
Decision Date1997-07-14
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TARGOBEAM is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1997-07-14 under 510(k) number K970819. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGOBEAM?

TARGOBEAM is a medical device that received FDA 510(k) clearance on 1997-07-14. The listed applicant is Ferguson Medical. The 510(k) number is K970819.

When did TARGOBEAM receive FDA 510(k) clearance?

TARGOBEAM received FDA 510(k) clearance on 1997-07-14, under 510(k) number K970819.

Who is the listed applicant for TARGOBEAM?

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 TARGOBEAM?

The FDA product code for TARGOBEAM is JAK.

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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.

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Related Devices (Code: JAK)

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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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