STORZ COMPUSCAN 68K
K-Number: K861335 · 1986-06-30
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Device Summary
Frequently Asked Questions
What is the STORZ COMPUSCAN 68K?
STORZ COMPUSCAN 68K is a medical device that received FDA 510(k) clearance on 1986-06-30. The listed applicant is Storz Instrument Co.. The 510(k) number is K861335.
When did STORZ COMPUSCAN 68K receive FDA 510(k) clearance?
STORZ COMPUSCAN 68K received FDA 510(k) clearance on 1986-06-30, under 510(k) number K861335.
Who is the listed applicant for STORZ COMPUSCAN 68K?
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 STORZ COMPUSCAN 68K?
The FDA product code for STORZ COMPUSCAN 68K 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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