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FDA 510(k)

WHITE CROSS STERILE PAD 4IN. X 4IN.

K-Number: K854809 · 1986-01-13

Decision Date1986-01-13
Product Code
DecisionSubstantially Equivalent

Device Summary

WHITE CROSS STERILE PAD 4IN. X 4IN. 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 1986-01-13 under 510(k) number K854809. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITE CROSS STERILE PAD 4IN. X 4IN.?

WHITE CROSS STERILE PAD 4IN. X 4IN. is a medical device that received FDA 510(k) clearance on 1986-01-13. The listed applicant is American White Cross, Inc.. The 510(k) number is K854809.

When did WHITE CROSS STERILE PAD 4IN. X 4IN. receive FDA 510(k) clearance?

WHITE CROSS STERILE PAD 4IN. X 4IN. received FDA 510(k) clearance on 1986-01-13, under 510(k) number K854809.

Who is the listed applicant for WHITE CROSS STERILE PAD 4IN. X 4IN.?

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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