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FDA 510(k)

MW STRAIGHT ATTACHMENT

K-Number: K792445 · 1979-12-06

ApplicantMidwest
Decision Date1979-12-06
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MW STRAIGHT ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792445. 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 MW STRAIGHT ATTACHMENT?

MW STRAIGHT ATTACHMENT is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Midwest. The 510(k) number is K792445.

When did MW STRAIGHT ATTACHMENT receive FDA 510(k) clearance?

MW STRAIGHT ATTACHMENT received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792445.

Who is the listed applicant for MW STRAIGHT ATTACHMENT?

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

What is the FDA product code for MW STRAIGHT ATTACHMENT?

The FDA product code for MW STRAIGHT ATTACHMENT is EGS.

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 Midwest 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.

K863677TRADITION HIGH SPEED HANDPIECEK850344AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANGK792304MW-8000K792302LS-100K792303MW 8000-IK791771ORALUMINATOR III AUTO-LIGHT

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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.K220346Lotus Prophy AngleAjk Engineering, 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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