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FDA 510(k)

PERIODONTAL PROBE - AUTOPROBE

K-Number: K880209 · 1988-04-27

ApplicantDentsply Intl.
Decision Date1988-04-27
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIODONTAL PROBE - AUTOPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1988-04-27 under 510(k) number K880209. The device is classified under product code EIL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIODONTAL PROBE - AUTOPROBE?

PERIODONTAL PROBE - AUTOPROBE is a medical device that received FDA 510(k) clearance on 1988-04-27. The listed applicant is Dentsply Intl.. The 510(k) number is K880209.

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

PERIODONTAL PROBE - AUTOPROBE received FDA 510(k) clearance on 1988-04-27, under 510(k) number K880209.

Who is the listed applicant for PERIODONTAL PROBE - AUTOPROBE?

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

What is the FDA product code for PERIODONTAL PROBE - AUTOPROBE?

The FDA product code for PERIODONTAL PROBE - AUTOPROBE is EIL.

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Related Devices (Code: EIL)

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.

K911643ABIODENT PERIOTEMP(R) SYSTEMAbiomed, Inc.K890493FLORIDA PROBE PERIODONTAL PROBEFlorida Probe Corp.K885075ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.K884813MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley ResearchK872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.K872215PERIO-TESTDr. Bernard Loewenthal

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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