WET PACK LINE OF PRODUCTS
K-Number: K820587 · 1982-03-26
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Device Summary
Frequently Asked Questions
What is the WET PACK LINE OF PRODUCTS?
WET PACK LINE OF PRODUCTS is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K820587.
When did WET PACK LINE OF PRODUCTS receive FDA 510(k) clearance?
WET PACK LINE OF PRODUCTS received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820587.
Who is the listed applicant for WET PACK LINE OF PRODUCTS?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WET PACK LINE OF PRODUCTS?
The FDA product code for WET PACK LINE OF PRODUCTS is KMJ.
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 Abco Dealers, 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.
Related Devices (Code: KMJ)
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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