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FDA 510(k)

PENCIL SKIN ABRADER

K-Number: K830663 · 1983-04-28

ApplicantNdm Corp.
Decision Date1983-04-28
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PENCIL SKIN ABRADER is the device name listed in this FDA 510(k) record. The listed applicant is Ndm Corp.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830663. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENCIL SKIN ABRADER?

PENCIL SKIN ABRADER is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Ndm Corp.. The 510(k) number is K830663.

When did PENCIL SKIN ABRADER receive FDA 510(k) clearance?

PENCIL SKIN ABRADER received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830663.

Who is the listed applicant for PENCIL SKIN ABRADER?

The FDA 510(k) record lists Ndm Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENCIL SKIN ABRADER?

The FDA product code for PENCIL SKIN ABRADER is DRX.

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Related Devices (Code: DRX)

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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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