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FDA 510(k)

BON APATITE HA PARTICLES

K-Number: K934430 · 1994-05-18

Decision Date1994-05-18
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BON APATITE HA PARTICLES is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Interfaces, Inc.. It received FDA 510(k) clearance on 1994-05-18 under 510(k) number K934430. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BON APATITE HA PARTICLES?

BON APATITE HA PARTICLES is a medical device that received FDA 510(k) clearance on 1994-05-18. The listed applicant is Bio-Interfaces, Inc.. The 510(k) number is K934430.

When did BON APATITE HA PARTICLES receive FDA 510(k) clearance?

BON APATITE HA PARTICLES received FDA 510(k) clearance on 1994-05-18, under 510(k) number K934430.

Who is the listed applicant for BON APATITE HA PARTICLES?

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

What is the FDA product code for BON APATITE HA PARTICLES?

The FDA product code for BON APATITE HA PARTICLES is LYC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Bio-Interfaces, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 17 devices →

Related Devices (Code: LYC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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