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FDA 510(k)

LIGHT, INSIDE

K-Number: K781878 · 1978-12-29

ApplicantMidwest
Decision Date1978-12-29
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT, INSIDE is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1978-12-29 under 510(k) number K781878. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT, INSIDE?

LIGHT, INSIDE is a medical device that received FDA 510(k) clearance on 1978-12-29. The listed applicant is Midwest. The 510(k) number is K781878.

When did LIGHT, INSIDE receive FDA 510(k) clearance?

LIGHT, INSIDE received FDA 510(k) clearance on 1978-12-29, under 510(k) number K781878.

Who is the listed applicant for LIGHT, INSIDE?

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 LIGHT, INSIDE?

The FDA product code for LIGHT, INSIDE is EAY.

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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 ANGK792445MW STRAIGHT ATTACHMENTK792304MW-8000K792302LS-100K792303MW 8000-I

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Related Devices (Code: EAY)

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.

K953192MODEL A15-103Beaverstate Dental, Inc.K953191MODEL A15-101Beaverstate Dental, Inc.K935718JEDENTAL VLC DENTAL CURING LIGHTJedental Co., Inc.K871816STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TMStryker Corp.K831976POWER OPTICRitter Co.K831824DENTAL ELECTRONIC/S.B.R TRADING BU HANDSilverman'S

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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