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FDA 510(k)

ANGIO WASTE FLUIDS DUMP BAG

K-Number: K874037 · 1988-01-29

ApplicantProcedure Products, Inc.
Decision Date1988-01-29
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIO WASTE FLUIDS DUMP BAG is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Products, Inc.. It received FDA 510(k) clearance on 1988-01-29 under 510(k) number K874037. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIO WASTE FLUIDS DUMP BAG?

ANGIO WASTE FLUIDS DUMP BAG is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Procedure Products, Inc.. The 510(k) number is K874037.

When did ANGIO WASTE FLUIDS DUMP BAG receive FDA 510(k) clearance?

ANGIO WASTE FLUIDS DUMP BAG received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874037.

Who is the listed applicant for ANGIO WASTE FLUIDS DUMP BAG?

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

What is the FDA product code for ANGIO WASTE FLUIDS DUMP BAG?

The FDA product code for ANGIO WASTE FLUIDS DUMP BAG is DQO.

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Related Devices (Code: DQO)

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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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