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FDA 510(k)

CERESTORE CORE MATERIAL

K-Number: K832286 · 1983-09-26

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1983-09-26
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERESTORE CORE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832286. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERESTORE CORE MATERIAL?

CERESTORE CORE MATERIAL is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K832286.

When did CERESTORE CORE MATERIAL receive FDA 510(k) clearance?

CERESTORE CORE MATERIAL received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832286.

Who is the listed applicant for CERESTORE CORE MATERIAL?

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

What is the FDA product code for CERESTORE CORE MATERIAL?

The FDA product code for CERESTORE CORE MATERIAL is EIH.

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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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