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FDA 510(k)

ACCUTEK PERIODONTAL PROBE

K-Number: K880827 · 1988-04-12

ApplicantSweet Micro Systems, Inc.
Decision Date1988-04-12
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCUTEK PERIODONTAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Sweet Micro Systems, Inc.. It received FDA 510(k) clearance on 1988-04-12 under 510(k) number K880827. 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 ACCUTEK PERIODONTAL PROBE?

ACCUTEK PERIODONTAL PROBE is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is Sweet Micro Systems, Inc.. The 510(k) number is K880827.

When did ACCUTEK PERIODONTAL PROBE receive FDA 510(k) clearance?

ACCUTEK PERIODONTAL PROBE received FDA 510(k) clearance on 1988-04-12, under 510(k) number K880827.

Who is the listed applicant for ACCUTEK PERIODONTAL PROBE?

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

What is the FDA product code for ACCUTEK PERIODONTAL PROBE?

The FDA product code for ACCUTEK PERIODONTAL PROBE 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.K875076FLORIDA PROBEFlorida Probe Corp.K870280ACCUDENT ACCUPROBEAccudent, Inc.

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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