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FDA 510(k)

SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL

K-Number: K913401 · 1992-03-06

ApplicantSmith & Nephew Dyonics, Inc.
Decision Date1992-03-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Dyonics, Inc.. It received FDA 510(k) clearance on 1992-03-06 under 510(k) number K913401. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL?

SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL is a medical device that received FDA 510(k) clearance on 1992-03-06. The listed applicant is Smith & Nephew Dyonics, Inc.. The 510(k) number is K913401.

When did SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL receive FDA 510(k) clearance?

SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL received FDA 510(k) clearance on 1992-03-06, under 510(k) number K913401.

Who is the listed applicant for SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL?

The FDA 510(k) record lists Smith & Nephew Dyonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL?

The FDA product code for SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL is HRX.

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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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