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FDA 510(k)

FIBER OPTIC ILLUMINATOR

K-Number: K801591 · 1980-07-21

ApplicantLares Manufacturing Co., Inc.
Decision Date1980-07-21
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lares Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801591. 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 FIBER OPTIC ILLUMINATOR?

FIBER OPTIC ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Lares Manufacturing Co., Inc.. The 510(k) number is K801591.

When did FIBER OPTIC ILLUMINATOR receive FDA 510(k) clearance?

FIBER OPTIC ILLUMINATOR received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801591.

Who is the listed applicant for FIBER OPTIC ILLUMINATOR?

The FDA 510(k) record lists Lares Manufacturing Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBER OPTIC ILLUMINATOR?

The FDA product code for FIBER OPTIC ILLUMINATOR is EAY.

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 Lares Manufacturing Co., 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.

K831351PERMALUX VISIBLE CURE COMPOSITE RESTORK801535LARES HANDPIECE OILK801592FIBER OPTIC HOSEK801534LARES AIR PRESSURE GAUGEK780038DENTAL HANDPIECE

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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