OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU
K-Number: K861535 · 1986-05-14
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Device Summary
Frequently Asked Questions
What is the OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU?
OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU is a medical device that received FDA 510(k) clearance on 1986-05-14. The listed applicant is CooperVision, Inc.. The 510(k) number is K861535.
When did OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU receive FDA 510(k) clearance?
OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU received FDA 510(k) clearance on 1986-05-14, under 510(k) number K861535.
Who is the listed applicant for OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU?
The FDA product code for OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU is HMR.
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 CooperVision, 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: HMR)
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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