NON WETTING UNDERCAST PADDING
K-Number: K833732 · 1983-12-12
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Device Summary
Frequently Asked Questions
What is the NON WETTING UNDERCAST PADDING?
NON WETTING UNDERCAST PADDING is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is American Medical Disposable, Inc.. The 510(k) number is K833732.
When did NON WETTING UNDERCAST PADDING receive FDA 510(k) clearance?
NON WETTING UNDERCAST PADDING received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833732.
Who is the listed applicant for NON WETTING UNDERCAST PADDING?
The FDA 510(k) record lists American Medical Disposable, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON WETTING UNDERCAST PADDING?
The FDA product code for NON WETTING UNDERCAST PADDING is ITG.
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 Medical Disposable, 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: ITG)
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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