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FDA 510(k)

PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR

K-Number: K871344 · 1987-10-20

ApplicantReynolds Medical , Ltd.
Decision Date1987-10-20
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR is the device name listed in this FDA 510(k) record. The listed applicant is Reynolds Medical , Ltd.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K871344. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR?

PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Reynolds Medical , Ltd.. The 510(k) number is K871344.

When did PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR receive FDA 510(k) clearance?

PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR received FDA 510(k) clearance on 1987-10-20, under 510(k) number K871344.

Who is the listed applicant for PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR?

The FDA 510(k) record lists Reynolds Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR?

The FDA product code for PATHFINDER 3, AUTO SURVEYOR AND SURVEYOR is DSI.

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Other records listing Reynolds Medical , Ltd. as applicant

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Related Devices (Code: DSI)

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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.

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