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FDA 510(k)

ALBA DRY BURN PAD

K-Number: K850881 · 1985-04-17

ApplicantAlba Health Care
Decision Date1985-04-17
Product Code
DecisionSubstantially Equivalent

Device Summary

ALBA DRY BURN PAD is the device name listed in this FDA 510(k) record. The listed applicant is Alba Health Care. It received FDA 510(k) clearance on 1985-04-17 under 510(k) number K850881. 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 1985-04-17. The listed applicant is Alba Health Care. The 510(k) number is K850881.

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

ALBA DRY BURN PAD received FDA 510(k) clearance on 1985-04-17, under 510(k) number K850881.

Who is the listed applicant for ALBA DRY BURN PAD?

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

Other records listing Alba Health Care 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.

K864689ALBA HEALTH CARE IODOFORM PACKING STRIPK861154ALBA HEALTH CARE PLAIN PACKING STRIPK851918INFANT PHOTOTHERAPY MASKK850904ALBA DRY BURN DRESSINGK850241ALBA HEALTH CARE NON-ADHERING DRESSINGK812904STERILE ORTHOPEDIC STOCKINETTE

View all 8 devices →

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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