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FDA 510(k)

JOY LIGHT

K-Number: K771249 · 1977-07-15

ApplicantM.D. Intl., Inc.
Decision Date1977-07-15
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JOY LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is M.D. Intl., Inc.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K771249. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOY LIGHT?

JOY LIGHT is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is M.D. Intl., Inc.. The 510(k) number is K771249.

When did JOY LIGHT receive FDA 510(k) clearance?

JOY LIGHT received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771249.

Who is the listed applicant for JOY LIGHT?

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

What is the FDA product code for JOY LIGHT?

The FDA product code for JOY LIGHT is EAZ.

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 M.D. Intl., Inc. 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.

K894788DMI SERIES 90 EXAMINATION TABLEK894789DMI 250 SERIES POWER SURGERY TABLEK870832OXY-THERM

Related Devices (Code: EAZ)

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.

K072309MICROLUX/BLUAddent, Inc.K041614MICROLUX DLAddent, Inc.K033033VIZILITE-BLUE ORAL EXAM KITTrylon Corp.K003995SPECULITE/ORALLITETrylon Corp.K926081DENTAL LIGHTMdt Corp., Inc.K935390SIROLUX FANTASTICPelton & Crane Co.

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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