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FDA 510(k)

DISPOSABLE PROPHY ANGLE

K-Number: K941009 · 1994-06-06

ApplicantAllpro, Inc.
Decision Date1994-06-06
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Allpro, Inc.. It received FDA 510(k) clearance on 1994-06-06 under 510(k) number K941009. 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 DISPOSABLE PROPHY ANGLE?

DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is Allpro, Inc.. The 510(k) number is K941009.

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

DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1994-06-06, under 510(k) number K941009.

Who is the listed applicant for DISPOSABLE PROPHY ANGLE?

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

What is the FDA product code for DISPOSABLE PROPHY ANGLE?

The FDA product code for DISPOSABLE PROPHY ANGLE is EGS.

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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

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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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