RETINAL TAAK
K-Number: K901275 · 1990-03-23
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Device Summary
Frequently Asked Questions
What is the RETINAL TAAK?
RETINAL TAAK is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Alcon Surgical, Inc.. The 510(k) number is K901275.
When did RETINAL TAAK receive FDA 510(k) clearance?
RETINAL TAAK received FDA 510(k) clearance on 1990-03-23, under 510(k) number K901275.
Who is the listed applicant for RETINAL TAAK?
The FDA 510(k) record lists Alcon Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RETINAL TAAK?
The FDA product code for RETINAL TAAK is HQW.
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 Alcon Surgical, 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: HQW)
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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