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FDA 510(k)

MARTIN COLD LIGHT FOUNTAIN

K-Number: K932060 · 1994-03-30

ApplicantMedline
Decision Date1994-03-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MARTIN COLD LIGHT FOUNTAIN is the device name listed in this FDA 510(k) record. The listed applicant is Medline. It received FDA 510(k) clearance on 1994-03-30 under 510(k) number K932060. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN COLD LIGHT FOUNTAIN?

MARTIN COLD LIGHT FOUNTAIN is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Medline. The 510(k) number is K932060.

When did MARTIN COLD LIGHT FOUNTAIN receive FDA 510(k) clearance?

MARTIN COLD LIGHT FOUNTAIN received FDA 510(k) clearance on 1994-03-30, under 510(k) number K932060.

Who is the listed applicant for MARTIN COLD LIGHT FOUNTAIN?

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

What is the FDA product code for MARTIN COLD LIGHT FOUNTAIN?

The FDA product code for MARTIN COLD LIGHT FOUNTAIN is GCJ.

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Related Devices (Code: GCJ)

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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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