NON-ADHERENT PAD
K-Number: K852412 · 1985-07-29
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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