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FDA 510(k)

ULTRA-LUX LIGHT SOURCE

K-Number: K870898 · 1987-03-18

ApplicantMedline Industries, Inc.
Decision Date1987-03-18
Product CodeFSW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRA-LUX LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1987-03-18 under 510(k) number K870898. The device is classified under product code FSW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-LUX LIGHT SOURCE?

ULTRA-LUX LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1987-03-18. The listed applicant is Medline Industries, Inc.. The 510(k) number is K870898.

When did ULTRA-LUX LIGHT SOURCE receive FDA 510(k) clearance?

ULTRA-LUX LIGHT SOURCE received FDA 510(k) clearance on 1987-03-18, under 510(k) number K870898.

Who is the listed applicant for ULTRA-LUX LIGHT SOURCE?

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

What is the FDA product code for ULTRA-LUX LIGHT SOURCE?

The FDA product code for ULTRA-LUX LIGHT SOURCE is FSW.

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Related Devices (Code: FSW)

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K022989RADLITE TISSUE RETRACTOR SYSTEMGenzyme BiosurgeryK013511XENALIGHT MODELS # AX9125 (100-120V~); # AX9225 (220-240V~)Aculux, Inc.K943342MEDICAM XENON LIGHT SOURCEM.P. Video, Inc.K934337CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCECuda Products Co.K922279ILLUMINATOR IV MINOR SURGERY LIGHTMedical Illumination, Inc.K913135LM-300TWINLeisegang Medical, 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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