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FDA 510(k)

AES STOCKINGS

K-Number: K822446 · 1982-08-27

Decision Date1982-08-27
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AES STOCKINGS is the device name listed in this FDA 510(k) record. The listed applicant is Rampon Products. It received FDA 510(k) clearance on 1982-08-27 under 510(k) number K822446. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AES STOCKINGS?

AES STOCKINGS is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Rampon Products. The 510(k) number is K822446.

When did AES STOCKINGS receive FDA 510(k) clearance?

AES STOCKINGS received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822446.

Who is the listed applicant for AES STOCKINGS?

The FDA 510(k) record lists Rampon Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AES STOCKINGS?

The FDA product code for AES STOCKINGS is DWL.

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.

Related Devices (Code: DWL)

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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