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FDA 510(k)

PASTE, PRO CARE PROPHYLAXIS

K-Number: K782104 · 1979-01-03

ApplicantYoung Dental Manufacturing Co. 1, LLC
Decision Date1979-01-03
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PASTE, PRO CARE PROPHYLAXIS is the device name listed in this FDA 510(k) record. The listed applicant is Young Dental Manufacturing Co. 1, LLC. It received FDA 510(k) clearance on 1979-01-03 under 510(k) number K782104. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PASTE, PRO CARE PROPHYLAXIS?

PASTE, PRO CARE PROPHYLAXIS is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is Young Dental Manufacturing Co. 1, LLC. The 510(k) number is K782104.

When did PASTE, PRO CARE PROPHYLAXIS receive FDA 510(k) clearance?

PASTE, PRO CARE PROPHYLAXIS received FDA 510(k) clearance on 1979-01-03, under 510(k) number K782104.

Who is the listed applicant for PASTE, PRO CARE PROPHYLAXIS?

The FDA 510(k) record lists Young Dental Manufacturing Co. 1, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PASTE, PRO CARE PROPHYLAXIS?

The FDA product code for PASTE, PRO CARE PROPHYLAXIS is FZE.

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Other records listing Young Dental Manufacturing Co. 1, LLC 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.

K241041Silver Fluoride Hypersensitivity VarnishK201127DEFEND Ear-loop Face MasksK171377Young INFINITY Cordless Handpiece SystemK153334Oral-B 5% Sodium Fluoride VarnishK932255YOUNG D'GRANULATORK903284YOUNG PROPHY SYSTEM, PS UNIT

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Related Devices (Code: FZE)

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.

K241253Medicon Epiplating SystemCmf Medicon Surgical, Inc.K161548Osseointegrated FixturesSouthern Implants (Pty), Ltd.K090803HANSON MEDICAL FACIAL IMPLANTSHanson Medical, Inc.K090630NOBEL BIOCARE ENDOSSEOUS IMPLANTS (MAXILLOFACIAL INDICATION)Nobel Biocare ABK071018MONARCH NASAL IMPLANTHanson Medical, Inc.K041690MONARCH NASAL IMPLANTHanson Medical, Inc.

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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