MAGNILINK SYSTEM 402/5
K-Number: K892350 · 1989-05-26
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Device Summary
Frequently Asked Questions
What is the MAGNILINK SYSTEM 402/5?
MAGNILINK SYSTEM 402/5 is a medical device that received FDA 510(k) clearance on 1989-05-26. The listed applicant is Coburn Optical Ind., Inc.. The 510(k) number is K892350.
When did MAGNILINK SYSTEM 402/5 receive FDA 510(k) clearance?
MAGNILINK SYSTEM 402/5 received FDA 510(k) clearance on 1989-05-26, under 510(k) number K892350.
Who is the listed applicant for MAGNILINK SYSTEM 402/5?
The FDA 510(k) record lists Coburn Optical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGNILINK SYSTEM 402/5?
The FDA product code for MAGNILINK SYSTEM 402/5 is HJG.
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 Coburn Optical Ind., 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: HJG)
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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