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FDA 510(k)

MW 8000-I

K-Number: K792303 · 1979-11-27

ApplicantMidwest
Decision Date1979-11-27
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MW 8000-I is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1979-11-27 under 510(k) number K792303. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MW 8000-I?

MW 8000-I is a medical device that received FDA 510(k) clearance on 1979-11-27. The listed applicant is Midwest. The 510(k) number is K792303.

When did MW 8000-I receive FDA 510(k) clearance?

MW 8000-I received FDA 510(k) clearance on 1979-11-27, under 510(k) number K792303.

Who is the listed applicant for MW 8000-I?

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 8000-I?

The FDA product code for MW 8000-I is EBF.

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 ANGK792445MW STRAIGHT ATTACHMENTK792304MW-8000K792302LS-100K791771ORALUMINATOR III AUTO-LIGHT

View all 13 devices →

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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