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FDA 510(k)

FLORIDA PROBE PERIODONTAL PROBE

K-Number: K890493 · 1989-03-13

ApplicantFlorida Probe Corp.
Decision Date1989-03-13
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLORIDA PROBE PERIODONTAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Florida Probe Corp.. It received FDA 510(k) clearance on 1989-03-13 under 510(k) number K890493. 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 FLORIDA PROBE PERIODONTAL PROBE?

FLORIDA PROBE PERIODONTAL PROBE is a medical device that received FDA 510(k) clearance on 1989-03-13. The listed applicant is Florida Probe Corp.. The 510(k) number is K890493.

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

FLORIDA PROBE PERIODONTAL PROBE received FDA 510(k) clearance on 1989-03-13, under 510(k) number K890493.

Who is the listed applicant for FLORIDA PROBE PERIODONTAL PROBE?

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

What is the FDA product code for FLORIDA PROBE PERIODONTAL PROBE?

The FDA product code for FLORIDA PROBE PERIODONTAL 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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Other records listing Florida Probe Corp. as applicant

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.

K875076FLORIDA PROBE

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.K885075ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.K884813MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley ResearchK880209PERIODONTAL 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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