FDA 510(k)

PRO-V

K-Number: K073263 · 2008-02-14

Decision Date2008-02-14

Product CodeEBG

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PRO-V is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 2008-02-14 under 510(k) number K073263. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-V?

PRO-V is a medical device that received FDA 510(k) clearance on 2008-02-14. The listed applicant is Bisco, Inc.. The 510(k) number is K073263.

When did PRO-V receive FDA 510(k) clearance?

PRO-V received FDA 510(k) clearance on 2008-02-14, under 510(k) number K073263.

Who is the listed applicant for PRO-V?

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

What is the FDA product code for PRO-V?

The FDA product code for PRO-V is EBG.

Other records listing Bisco, Inc. as applicant

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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.