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FDA 510(k)

WATER RESISTANT FOOTSWITCH W/CABLE

K-Number: K810101 · 1981-01-29

ApplicantAspen Laboratories, Inc.
Decision Date1981-01-29
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WATER RESISTANT FOOTSWITCH W/CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1981-01-29 under 510(k) number K810101. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER RESISTANT FOOTSWITCH W/CABLE?

WATER RESISTANT FOOTSWITCH W/CABLE is a medical device that received FDA 510(k) clearance on 1981-01-29. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K810101.

When did WATER RESISTANT FOOTSWITCH W/CABLE receive FDA 510(k) clearance?

WATER RESISTANT FOOTSWITCH W/CABLE received FDA 510(k) clearance on 1981-01-29, under 510(k) number K810101.

Who is the listed applicant for WATER RESISTANT FOOTSWITCH W/CABLE?

The FDA 510(k) record lists Aspen Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATER RESISTANT FOOTSWITCH W/CABLE?

The FDA product code for WATER RESISTANT FOOTSWITCH W/CABLE is GEI.

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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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