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FDA 510(k)

THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.)

K-Number: K920455 · 1992-03-31

Decision Date1992-03-31
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THERAVIEW DIGITAL PORTAL IMAGING COMPUTER (MOD.) is the device name listed in this FDA 510(k) record. The listed applicant is S & S Inficon, Inc.. It received FDA 510(k) clearance on 1992-03-31 under 510(k) number K920455. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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