Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PORTRAIT PSR, MODEL 745915

K-Number: K073111 · 2008-03-27

Decision Date2008-03-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTRAIT PSR, MODEL 745915 is the device name listed in this FDA 510(k) record. The listed applicant is Rhytec Incorporated. It received FDA 510(k) clearance on 2008-03-27 under 510(k) number K073111. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTRAIT PSR, MODEL 745915?

PORTRAIT PSR, MODEL 745915 is a medical device that received FDA 510(k) clearance on 2008-03-27. The listed applicant is Rhytec Incorporated. The 510(k) number is K073111.

When did PORTRAIT PSR, MODEL 745915 receive FDA 510(k) clearance?

PORTRAIT PSR, MODEL 745915 received FDA 510(k) clearance on 2008-03-27, under 510(k) number K073111.

Who is the listed applicant for PORTRAIT PSR, MODEL 745915?

The FDA 510(k) record lists Rhytec Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTRAIT PSR, MODEL 745915?

The FDA product code for PORTRAIT PSR, MODEL 745915 is GEI.

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 Rhytec Incorporated 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: GEI)

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.

↑