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FDA 510(k)

NON - ADHERENT BANDAGE

K-Number: K833733 · 1983-12-27

Decision Date1983-12-27
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

NON - ADHERENT BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Disposable, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833733. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON - ADHERENT BANDAGE?

NON - ADHERENT BANDAGE is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is American Medical Disposable, Inc.. The 510(k) number is K833733.

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

NON - ADHERENT BANDAGE received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833733.

Who is the listed applicant for NON - ADHERENT BANDAGE?

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 - ADHERENT BANDAGE?

The FDA product code for NON - ADHERENT BANDAGE is FRO. This falls under the Anesthesiology category.

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.

View all 33 devices →

Related Devices (Code: FRO)

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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