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FDA 510(k)

PROVIDENCE CUP SYSTEM

K-Number: K990821 · 1999-04-29

ApplicantBiopro, Inc.
Decision Date1999-04-29
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROVIDENCE CUP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biopro, Inc.. It received FDA 510(k) clearance on 1999-04-29 under 510(k) number K990821. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROVIDENCE CUP SYSTEM?

PROVIDENCE CUP SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-29. The listed applicant is Biopro, Inc.. The 510(k) number is K990821.

When did PROVIDENCE CUP SYSTEM receive FDA 510(k) clearance?

PROVIDENCE CUP SYSTEM received FDA 510(k) clearance on 1999-04-29, under 510(k) number K990821.

Who is the listed applicant for PROVIDENCE CUP SYSTEM?

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

What is the FDA product code for PROVIDENCE CUP SYSTEM?

The FDA product code for PROVIDENCE CUP SYSTEM is JDI.

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Related Devices (Code: JDI)

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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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