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FDA 510(k)

ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES

K-Number: K900178 · 1990-05-31

ApplicantCore-Vent Corp.
Decision Date1990-05-31
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES is the device name listed in this FDA 510(k) record. The listed applicant is Core-Vent Corp.. It received FDA 510(k) clearance on 1990-05-31 under 510(k) number K900178. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES?

ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES is a medical device that received FDA 510(k) clearance on 1990-05-31. The listed applicant is Core-Vent Corp.. The 510(k) number is K900178.

When did ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES receive FDA 510(k) clearance?

ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES received FDA 510(k) clearance on 1990-05-31, under 510(k) number K900178.

Who is the listed applicant for ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES?

The FDA 510(k) record lists Core-Vent Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES?

The FDA product code for ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES is EFS.

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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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