MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159
K-Number: K001698 · 2000-07-17
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Device Summary
Frequently Asked Questions
What is the MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159?
MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159 is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is Cogent Light Technologies, Inc.. The 510(k) number is K001698.
When did MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159 receive FDA 510(k) clearance?
MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159 received FDA 510(k) clearance on 2000-07-17, under 510(k) number K001698.
Who is the listed applicant for MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159?
The FDA 510(k) record lists Cogent Light Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159?
The FDA product code for MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159 is FFS.
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 Cogent Light Technologies, 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: FFS)
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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