DESIGNS FOR VISION FIBEROPTIC LIGHT
K-Number: K032283 · 2003-08-20
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Device Summary
Frequently Asked Questions
What is the DESIGNS FOR VISION FIBEROPTIC LIGHT?
DESIGNS FOR VISION FIBEROPTIC LIGHT is a medical device that received FDA 510(k) clearance on 2003-08-20. The listed applicant is Designs For Vision, Inc.. The 510(k) number is K032283.
When did DESIGNS FOR VISION FIBEROPTIC LIGHT receive FDA 510(k) clearance?
DESIGNS FOR VISION FIBEROPTIC LIGHT received FDA 510(k) clearance on 2003-08-20, under 510(k) number K032283.
Who is the listed applicant for DESIGNS FOR VISION FIBEROPTIC LIGHT?
The FDA 510(k) record lists Designs For Vision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DESIGNS FOR VISION FIBEROPTIC LIGHT?
The FDA product code for DESIGNS FOR VISION FIBEROPTIC LIGHT is GDB.
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 Designs For Vision, 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.
Related Devices (Code: GDB)
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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