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FDA 510(k)

TARGOGRID

K-Number: K970037 · 1997-03-12

ApplicantDaum GmbH
Decision Date1997-03-12
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TARGOGRID is the device name listed in this FDA 510(k) record. The listed applicant is Daum GmbH. It received FDA 510(k) clearance on 1997-03-12 under 510(k) number K970037. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGOGRID?

TARGOGRID is a medical device that received FDA 510(k) clearance on 1997-03-12. The listed applicant is Daum GmbH. The 510(k) number is K970037.

When did TARGOGRID receive FDA 510(k) clearance?

TARGOGRID received FDA 510(k) clearance on 1997-03-12, under 510(k) number K970037.

Who is the listed applicant for TARGOGRID?

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

What is the FDA product code for TARGOGRID?

The FDA product code for TARGOGRID is LNH.

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Other records listing Daum GmbH 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.

K010037DAUM DOUBLE-SHOOT BISOPSY GUNK991366DAUM MRI/CONVENTIONAL BIOPSY KITK990782DAUM NEUROGATE TROCAR

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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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