SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR
K-Number: K844357 · 1985-06-05
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Device Summary
Frequently Asked Questions
What is the SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR?
SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is Coherent Medical Group. The 510(k) number is K844357.
When did SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR receive FDA 510(k) clearance?
SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR received FDA 510(k) clearance on 1985-06-05, under 510(k) number K844357.
Who is the listed applicant for SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR?
The FDA 510(k) record lists Coherent Medical Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR?
The FDA product code for SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR is HQF.
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 Coherent Medical Group 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: HQF)
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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