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FDA 510(k)

FLUID PUMP, CP #3

K-Number: K914524 · 1994-03-09

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1994-03-09
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLUID PUMP, CP #3 is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K914524. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID PUMP, CP #3?

FLUID PUMP, CP #3 is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K914524.

When did FLUID PUMP, CP #3 receive FDA 510(k) clearance?

FLUID PUMP, CP #3 received FDA 510(k) clearance on 1994-03-09, under 510(k) number K914524.

Who is the listed applicant for FLUID PUMP, CP #3?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUID PUMP, CP #3?

The FDA product code for FLUID PUMP, CP #3 is FEB.

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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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