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FDA 510(k)

MIDKIFF GEOSTATIC CLAMP

K-Number: K925035 · 1993-02-18

Decision Date1993-02-18
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIDKIFF GEOSTATIC CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is D.L. Nelson and Assoc., Inc.. It received FDA 510(k) clearance on 1993-02-18 under 510(k) number K925035. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDKIFF GEOSTATIC CLAMP?

MIDKIFF GEOSTATIC CLAMP is a medical device that received FDA 510(k) clearance on 1993-02-18. The listed applicant is D.L. Nelson and Assoc., Inc.. The 510(k) number is K925035.

When did MIDKIFF GEOSTATIC CLAMP receive FDA 510(k) clearance?

MIDKIFF GEOSTATIC CLAMP received FDA 510(k) clearance on 1993-02-18, under 510(k) number K925035.

Who is the listed applicant for MIDKIFF GEOSTATIC CLAMP?

The FDA 510(k) record lists D.L. Nelson and Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDKIFF GEOSTATIC CLAMP?

The FDA product code for MIDKIFF GEOSTATIC CLAMP is FWZ.

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.

Other records listing D.L. Nelson and Assoc., 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.

Related Devices (Code: FWZ)

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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