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FDA 510(k)

BIOPHASE IMPLANT MATERIAL

K-Number: K792329 · 1980-01-23

ApplicantRichard'S Medical Equip., Inc.
Decision Date1980-01-23
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOPHASE IMPLANT MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1980-01-23 under 510(k) number K792329. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPHASE IMPLANT MATERIAL?

BIOPHASE IMPLANT MATERIAL is a medical device that received FDA 510(k) clearance on 1980-01-23. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K792329.

When did BIOPHASE IMPLANT MATERIAL receive FDA 510(k) clearance?

BIOPHASE IMPLANT MATERIAL received FDA 510(k) clearance on 1980-01-23, under 510(k) number K792329.

Who is the listed applicant for BIOPHASE IMPLANT MATERIAL?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPHASE IMPLANT MATERIAL?

The FDA product code for BIOPHASE IMPLANT MATERIAL is JDG.

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Related Devices (Code: JDG)

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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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