COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR
K-Number: K910956 · 1991-09-04
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Device Summary
Frequently Asked Questions
What is the COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR?
COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Storz Instrument Co.. The 510(k) number is K910956.
When did COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR receive FDA 510(k) clearance?
COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR received FDA 510(k) clearance on 1991-09-04, under 510(k) number K910956.
Who is the listed applicant for COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR?
The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR?
The FDA product code for COMPUSCAN LT BIOMETRIC RULER AND IOL CALCULATOR is IYO.
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 Storz Instrument Co. 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: IYO)
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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