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FDA 510(k)

MPS DIAMOND POLISHING GEL

K-Number: K903003 · 1990-08-29

ApplicantAbrasive Technology, Inc.
Decision Date1990-08-29
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MPS DIAMOND POLISHING GEL is the device name listed in this FDA 510(k) record. The listed applicant is Abrasive Technology, Inc.. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K903003. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPS DIAMOND POLISHING GEL?

MPS DIAMOND POLISHING GEL is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Abrasive Technology, Inc.. The 510(k) number is K903003.

When did MPS DIAMOND POLISHING GEL receive FDA 510(k) clearance?

MPS DIAMOND POLISHING GEL received FDA 510(k) clearance on 1990-08-29, under 510(k) number K903003.

Who is the listed applicant for MPS DIAMOND POLISHING GEL?

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

What is the FDA product code for MPS DIAMOND POLISHING GEL?

The FDA product code for MPS DIAMOND POLISHING GEL is EJR.

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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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