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FDA 510(k)

FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE

K-Number: K093192 · 2010-02-12

ApplicantAdvanced Vascular Dynamics
Decision Date2010-02-12
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Vascular Dynamics. It received FDA 510(k) clearance on 2010-02-12 under 510(k) number K093192. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE?

FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE is a medical device that received FDA 510(k) clearance on 2010-02-12. The listed applicant is Advanced Vascular Dynamics. The 510(k) number is K093192.

When did FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE receive FDA 510(k) clearance?

FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE received FDA 510(k) clearance on 2010-02-12, under 510(k) number K093192.

Who is the listed applicant for FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE?

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

What is the FDA product code for FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE?

The FDA product code for FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE is JOM.

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Other records listing Advanced Vascular Dynamics 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.

K092503RADAR VASCULAR COMPRESSION DEVICESK090286PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICEK072167COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICEK040615COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEM

Related Devices (Code: JOM)

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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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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