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FDA 510(k)

POST CEMENT HI-X

K-Number: K992248 · 1999-08-25

ApplicantBisco, Inc.
Decision Date1999-08-25
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POST CEMENT HI-X is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1999-08-25 under 510(k) number K992248. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST CEMENT HI-X?

POST CEMENT HI-X is a medical device that received FDA 510(k) clearance on 1999-08-25. The listed applicant is Bisco, Inc.. The 510(k) number is K992248.

When did POST CEMENT HI-X receive FDA 510(k) clearance?

POST CEMENT HI-X received FDA 510(k) clearance on 1999-08-25, under 510(k) number K992248.

Who is the listed applicant for POST CEMENT HI-X?

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 POST CEMENT HI-X?

The FDA product code for POST CEMENT HI-X is EBF.

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Other records listing Bisco, Inc. as applicant

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Related Devices (Code: EBF)

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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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