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FDA 510(k)

NON-ADHERENT PAD

K-Number: K852412 · 1985-07-29

Decision Date1985-07-29
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

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 1985-07-29 under 510(k) number K852412. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-ADHERENT PAD?

NON-ADHERENT PAD is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is American White Cross, Inc.. The 510(k) number is K852412.

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

NON-ADHERENT PAD received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852412.

Who is the listed applicant for 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.

What is the FDA product code for NON-ADHERENT PAD?

The FDA product code for NON-ADHERENT PAD is EFQ.

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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Related Devices (Code: EFQ)

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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