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FDA 510(k)

MINIDENTOFLEX NEW POLISHING SYSTEM

K-Number: K780376 · 1978-03-14

ApplicantCavitron Corp.
Decision Date1978-03-14
Product CodeEHL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINIDENTOFLEX NEW POLISHING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780376. The device is classified under product code EHL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIDENTOFLEX NEW POLISHING SYSTEM?

MINIDENTOFLEX NEW POLISHING SYSTEM is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Cavitron Corp.. The 510(k) number is K780376.

When did MINIDENTOFLEX NEW POLISHING SYSTEM receive FDA 510(k) clearance?

MINIDENTOFLEX NEW POLISHING SYSTEM received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780376.

Who is the listed applicant for MINIDENTOFLEX NEW POLISHING SYSTEM?

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

What is the FDA product code for MINIDENTOFLEX NEW POLISHING SYSTEM?

The FDA product code for MINIDENTOFLEX NEW POLISHING SYSTEM is EHL.

Related Clinical Trials

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Other records listing Cavitron 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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Related Devices (Code: EHL)

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.

K792250CUTTER POINTSCutter Laboratories, Inc.K780811DENTAL ABRASIVE DEVICECavitron Corp.K780377PINIDENTOFLEX DENTAL POLISHERCavitron Corp.

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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