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FDA 510(k)

R.L. MEDICAL TWIN LIGHT SOURCE

K-Number: K842609 · 1984-08-09

ApplicantTridak Division of Indicon, Inc.
Decision Date1984-08-09
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

R.L. MEDICAL TWIN LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Tridak Division of Indicon, Inc.. It received FDA 510(k) clearance on 1984-08-09 under 510(k) number K842609. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R.L. MEDICAL TWIN LIGHT SOURCE?

R.L. MEDICAL TWIN LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1984-08-09. The listed applicant is Tridak Division of Indicon, Inc.. The 510(k) number is K842609.

When did R.L. MEDICAL TWIN LIGHT SOURCE receive FDA 510(k) clearance?

R.L. MEDICAL TWIN LIGHT SOURCE received FDA 510(k) clearance on 1984-08-09, under 510(k) number K842609.

Who is the listed applicant for R.L. MEDICAL TWIN LIGHT SOURCE?

The FDA 510(k) record lists Tridak Division of Indicon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R.L. MEDICAL TWIN LIGHT SOURCE?

The FDA product code for R.L. MEDICAL TWIN LIGHT SOURCE is FCW.

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Other records listing Tridak Division of Indicon, Inc. as applicant

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Related Devices (Code: FCW)

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K123956POWER LED 175KARL STORZ Endoscopy-America, Inc.K123359OVS1 VIDEO SYSTEMOlive Medical Corp.K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2Richard Wolf Medical Instruments Corp.K093792LED LIGHT SOURCESunoptic Technologies, LLCK091968KARL STORZ LED NOVA 100 COLD LIGHT FOUNTAIN, MODELS 2016020, 20161020CKARL STORZ Endoscopy-America, Inc.K082813STRYKER LED LIGHTSOURCEStryker Corp.

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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