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FDA 510(k)

WET-STOP

K-Number: K842547 · 1984-10-19

Decision Date1984-10-19
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WET-STOP is the device name listed in this FDA 510(k) record. The listed applicant is Palco Laboratories, Inc.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K842547. The device is classified under product code KPN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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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