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FDA 510(k)

MODEL 200A ELECTRONIC FORCE-SENSING PROBE

K-Number: K884813 · 1989-01-05

ApplicantVine Valley Research
Decision Date1989-01-05
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL 200A ELECTRONIC FORCE-SENSING PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Vine Valley Research. It received FDA 510(k) clearance on 1989-01-05 under 510(k) number K884813. 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 MODEL 200A ELECTRONIC FORCE-SENSING PROBE?

MODEL 200A ELECTRONIC FORCE-SENSING PROBE is a medical device that received FDA 510(k) clearance on 1989-01-05. The listed applicant is Vine Valley Research. The 510(k) number is K884813.

When did MODEL 200A ELECTRONIC FORCE-SENSING PROBE receive FDA 510(k) clearance?

MODEL 200A ELECTRONIC FORCE-SENSING PROBE received FDA 510(k) clearance on 1989-01-05, under 510(k) number K884813.

Who is the listed applicant for MODEL 200A ELECTRONIC FORCE-SENSING PROBE?

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

What is the FDA product code for MODEL 200A ELECTRONIC FORCE-SENSING PROBE?

The FDA product code for MODEL 200A ELECTRONIC FORCE-SENSING PROBE is EIL.

Related Clinical Trials

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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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.K880209PERIODONTAL PROBE - AUTOPROBEDentsply Intl.K872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.K872215PERIO-TESTDr. Bernard Loewenthal

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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