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FDA 510(k)

PINIDENTOFLEX DENTAL POLISHER

K-Number: K780377 · 1978-03-14

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

Device Summary

PINIDENTOFLEX DENTAL POLISHER 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 K780377. 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 PINIDENTOFLEX DENTAL POLISHER?

PINIDENTOFLEX DENTAL POLISHER 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 K780377.

When did PINIDENTOFLEX DENTAL POLISHER receive FDA 510(k) clearance?

PINIDENTOFLEX DENTAL POLISHER received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780377.

Who is the listed applicant for PINIDENTOFLEX DENTAL POLISHER?

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 PINIDENTOFLEX DENTAL POLISHER?

The FDA product code for PINIDENTOFLEX DENTAL POLISHER is EHL.

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 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

View all 32 devices →

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.K780376MINIDENTOFLEX NEW POLISHING SYSTEMCavitron 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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