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FDA 510(k)

3 X 4 NON-ADHERENT PAD

K-Number: K850595 · 1985-03-11

Decision Date1985-03-11
Product Code
DecisionSubstantially Equivalent

Device Summary

3 X 4 NON-ADHERENT PAD is the device name listed in this FDA 510(k) record. The listed applicant is American White Cross, Inc.. It received FDA 510(k) clearance on 1985-03-11 under 510(k) number K850595. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3 X 4 NON-ADHERENT PAD?

3 X 4 NON-ADHERENT PAD is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is American White Cross, Inc.. The 510(k) number is K850595.

When did 3 X 4 NON-ADHERENT PAD receive FDA 510(k) clearance?

3 X 4 NON-ADHERENT PAD received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850595.

Who is the listed applicant for 3 X 4 NON-ADHERENT PAD?

The FDA 510(k) record lists American White Cross, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 American White Cross, 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.

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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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