THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.)
K-Number: K920455 · 1992-03-31
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Device Summary
Frequently Asked Questions
What is the THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.)?
THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.) is a medical device that received FDA 510(k) clearance on 1992-03-31. The listed applicant is S & S Inficon, Inc.. The 510(k) number is K920455.
When did THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.) receive FDA 510(k) clearance?
THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.) received FDA 510(k) clearance on 1992-03-31, under 510(k) number K920455.
Who is the listed applicant for THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.)?
The FDA 510(k) record lists S & S Inficon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.)?
The FDA product code for THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.) is IYE.
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 S & S Inficon, 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: IYE)
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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