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FDA 510(k)

DENSCO PROPHY ANGLE

K-Number: K821686 · 1982-06-25

ApplicantTeledyne Densco
Decision Date1982-06-25
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENSCO PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Densco. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821686. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENSCO PROPHY ANGLE?

DENSCO PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Teledyne Densco. The 510(k) number is K821686.

When did DENSCO PROPHY ANGLE receive FDA 510(k) clearance?

DENSCO PROPHY ANGLE received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821686.

Who is the listed applicant for DENSCO PROPHY ANGLE?

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

What is the FDA product code for DENSCO PROPHY ANGLE?

The FDA product code for DENSCO PROPHY ANGLE is EGS.

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Other records listing Teledyne Densco 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.

K821364PROFLEX FLEXIBLE SCALERK803155PROPHYLAXIS CUP.K780641DENTAL ROTARY CARBIDE BURS 76EJL

Related Devices (Code: EGS)

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.

K251869Disposable Prophy Angle (3399-60, 3399-090, 3399-105)Premium Plus (Dongguan) LimitedK240950Disposable Prophy AnglePacific Care LimitedK240183Star E900 Handpiece SeriesDentalez, Inc., Stardental DivisionK230106General Cutting StraightNakanishi, Inc.K222518FX ContraNakanishi, Inc.K220874Smooth Drive contra angle and straight handpiecesLares Research

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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