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FDA 510(k)

ACCUDENT ACCUPROBE

K-Number: K870280 · 1987-06-08

ApplicantAccudent, Inc.
Decision Date1987-06-08
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCUDENT ACCUPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Accudent, Inc.. It received FDA 510(k) clearance on 1987-06-08 under 510(k) number K870280. The device is classified under product code EIX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUDENT ACCUPROBE?

ACCUDENT ACCUPROBE is a medical device that received FDA 510(k) clearance on 1987-06-08. The listed applicant is Accudent, Inc.. The 510(k) number is K870280.

When did ACCUDENT ACCUPROBE receive FDA 510(k) clearance?

ACCUDENT ACCUPROBE received FDA 510(k) clearance on 1987-06-08, under 510(k) number K870280.

Who is the listed applicant for ACCUDENT ACCUPROBE?

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

What is the FDA product code for ACCUDENT ACCUPROBE?

The FDA product code for ACCUDENT ACCUPROBE is EIX.

Related Clinical Trials

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Related Devices (Code: EIX)

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.

K960245VIP VICTOR INTERACTIVE PROBEPro-DentecK944848THE VIVACARE T.P.S. PROBERms Div.K936221PROBE TIP/PERI PROBE/PERI PROBE COMP.Pd International ABK890333ALBUMIN REAGENTAlpkem Corp.K880827ACCUTEK PERIODONTAL PROBESweet Micro Systems, Inc.K875076FLORIDA PROBEFlorida Probe Corp.

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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