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FDA 510(k)

PORTRAIT PSR

K-Number: K071786 · 2007-07-26

ApplicantRhytec Incorporated
Decision Date2007-07-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTRAIT PSR is the device name listed in this FDA 510(k) record. The listed applicant is Rhytec Incorporated. It received FDA 510(k) clearance on 2007-07-26 under 510(k) number K071786. 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?

PORTRAIT PSR is a medical device that received FDA 510(k) clearance on 2007-07-26. The listed applicant is Rhytec Incorporated. The 510(k) number is K071786.

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

PORTRAIT PSR received FDA 510(k) clearance on 2007-07-26, under 510(k) number K071786.

Who is the listed applicant for PORTRAIT PSR?

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?

The FDA product code for PORTRAIT PSR 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.

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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.

K082197RHYTEC, INC., PORTRAIT PSRK073111PORTRAIT PSR, MODEL 745915K072394PORTRAIT STAND-OFFK060948PORTRAIT PSR3

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.

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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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