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FDA 510(k)

ALBA DRY BURN PAD

K-Number: K852091 · 1985-06-13

Decision Date1985-06-13
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALBA DRY BURN PAD is the device name listed in this FDA 510(k) record. The listed applicant is Alba-Waldensian, Inc.. It received FDA 510(k) clearance on 1985-06-13 under 510(k) number K852091. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALBA DRY BURN PAD?

ALBA DRY BURN PAD is a medical device that received FDA 510(k) clearance on 1985-06-13. The listed applicant is Alba-Waldensian, Inc.. The 510(k) number is K852091.

When did ALBA DRY BURN PAD receive FDA 510(k) clearance?

ALBA DRY BURN PAD received FDA 510(k) clearance on 1985-06-13, under 510(k) number K852091.

Who is the listed applicant for ALBA DRY BURN PAD?

The FDA 510(k) record lists Alba-Waldensian, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALBA DRY BURN PAD?

The FDA product code for ALBA DRY BURN PAD is NAD.

Other records listing Alba-Waldensian, 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 8 devices →

Related Devices (Code: NAD)

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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