WET-STOP
K-Number: K842547 · 1984-10-19
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Device Summary
Frequently Asked Questions
What is the WET-STOP?
WET-STOP is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is Palco Laboratories, Inc.. The 510(k) number is K842547.
When did WET-STOP receive FDA 510(k) clearance?
WET-STOP received FDA 510(k) clearance on 1984-10-19, under 510(k) number K842547.
Who is the listed applicant for WET-STOP?
The FDA 510(k) record lists Palco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WET-STOP?
The FDA product code for WET-STOP is KPN.
Other records listing Palco Laboratories, 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: KPN)
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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