FIBEROPTIC LIGHTSOURCES AND CARRIERS
K-Number: K933145 · 1993-09-07
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Device Summary
Frequently Asked Questions
What is the FIBEROPTIC LIGHTSOURCES AND CARRIERS?
FIBEROPTIC LIGHTSOURCES AND CARRIERS is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Electro Fiberoptics Corp.. The 510(k) number is K933145.
When did FIBEROPTIC LIGHTSOURCES AND CARRIERS receive FDA 510(k) clearance?
FIBEROPTIC LIGHTSOURCES AND CARRIERS received FDA 510(k) clearance on 1993-09-07, under 510(k) number K933145.
Who is the listed applicant for FIBEROPTIC LIGHTSOURCES AND CARRIERS?
The FDA 510(k) record lists Electro Fiberoptics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIBEROPTIC LIGHTSOURCES AND CARRIERS?
The FDA product code for FIBEROPTIC LIGHTSOURCES AND CARRIERS is EQH.
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.
Other records listing Electro Fiberoptics Corp. 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.
Related Devices (Code: EQH)
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.
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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