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FDA 510(k)

INSPEKTOR PRO

K-Number: K040063 · 2004-06-24

ApplicantInspektor Dental Care BV
Decision Date2004-06-24
Product CodeNBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INSPEKTOR PRO is the device name listed in this FDA 510(k) record. The listed applicant is Inspektor Dental Care BV. It received FDA 510(k) clearance on 2004-06-24 under 510(k) number K040063. The device is classified under product code NBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPEKTOR PRO?

INSPEKTOR PRO is a medical device that received FDA 510(k) clearance on 2004-06-24. The listed applicant is Inspektor Dental Care BV. The 510(k) number is K040063.

When did INSPEKTOR PRO receive FDA 510(k) clearance?

INSPEKTOR PRO received FDA 510(k) clearance on 2004-06-24, under 510(k) number K040063.

Who is the listed applicant for INSPEKTOR PRO?

The FDA 510(k) record lists Inspektor Dental Care BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSPEKTOR PRO?

The FDA product code for INSPEKTOR PRO is NBL.

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Related Devices (Code: NBL)

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.

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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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