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FDA 510(k)

LIGHT-PAK

K-Number: K791733 · 1979-10-23

ApplicantMidwest
Decision Date1979-10-23
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT-PAK is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1979-10-23 under 510(k) number K791733. 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-PAK?

LIGHT-PAK is a medical device that received FDA 510(k) clearance on 1979-10-23. The listed applicant is Midwest. The 510(k) number is K791733.

When did LIGHT-PAK receive FDA 510(k) clearance?

LIGHT-PAK received FDA 510(k) clearance on 1979-10-23, under 510(k) number K791733.

Who is the listed applicant for LIGHT-PAK?

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-PAK?

The FDA product code for LIGHT-PAK 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.

K953191MODEL A15-101Beaverstate Dental, Inc.K953192MODEL A15-103Beaverstate 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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