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FDA 510(k)

BIOPRO 32MM BALL

K-Number: K872856 · 1987-08-17

ApplicantBiopro, Inc.
Decision Date1987-08-17
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOPRO 32MM BALL is the device name listed in this FDA 510(k) record. The listed applicant is Biopro, Inc.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K872856. 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 BIOPRO 32MM BALL?

BIOPRO 32MM BALL is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Biopro, Inc.. The 510(k) number is K872856.

When did BIOPRO 32MM BALL receive FDA 510(k) clearance?

BIOPRO 32MM BALL received FDA 510(k) clearance on 1987-08-17, under 510(k) number K872856.

Who is the listed applicant for BIOPRO 32MM BALL?

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 BIOPRO 32MM BALL?

The FDA product code for BIOPRO 32MM BALL is JDI.

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Other records listing Biopro, Inc. as applicant

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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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