FDA 510(k)

FEMORAL CANAL BRUSH

K-Number: K810267 · 1981-02-09

Decision Date1981-02-09

Product CodeLXH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

FEMORAL CANAL BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1981-02-09 under 510(k) number K810267. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL CANAL BRUSH?

FEMORAL CANAL BRUSH is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K810267.

When did FEMORAL CANAL BRUSH receive FDA 510(k) clearance?

FEMORAL CANAL BRUSH received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810267.

Who is the listed applicant for FEMORAL CANAL BRUSH?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMORAL CANAL BRUSH?

The FDA product code for FEMORAL CANAL BRUSH is LXH.

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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.