SOFTCARE BARRIER WET DRESSING
K-Number: K812736 · 1981-11-06
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Device Summary
Frequently Asked Questions
What is the SOFTCARE BARRIER WET DRESSING?
SOFTCARE BARRIER WET DRESSING is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is The Kendal Co.. The 510(k) number is K812736.
When did SOFTCARE BARRIER WET DRESSING receive FDA 510(k) clearance?
SOFTCARE BARRIER WET DRESSING received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812736.
Who is the listed applicant for SOFTCARE BARRIER WET DRESSING?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOFTCARE BARRIER WET DRESSING?
The FDA product code for SOFTCARE BARRIER WET DRESSING is EFQ.
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 The Kendal Co. 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: EFQ)
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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