FDA 510(k)

THE PATHFINDER

K-Number: K842304 · 1984-08-01

Decision Date1984-08-01

Product Code

DecisionSubstantially Equivalent

Device Summary

THE PATHFINDER is the device name listed in this FDA 510(k) record. The listed applicant is Hydro-Med Products, Inc.. It received FDA 510(k) clearance on 1984-08-01 under 510(k) number K842304. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PATHFINDER?

THE PATHFINDER is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Hydro-Med Products, Inc.. The 510(k) number is K842304.

When did THE PATHFINDER receive FDA 510(k) clearance?

THE PATHFINDER received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842304.

Who is the listed applicant for THE PATHFINDER?

The FDA 510(k) record lists Hydro-Med Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.