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FDA 510(k)

TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT

K-Number: K961368 · 1996-10-11

Decision Date1996-10-11
Product CodeDPT
Advisory CommitteeCV
DecisionUnknown

Device Summary

TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Vasamedics, LLC. It received FDA 510(k) clearance on 1996-10-11 under 510(k) number K961368. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT?

TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Vasamedics, LLC. The 510(k) number is K961368.

When did TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT receive FDA 510(k) clearance?

TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT received FDA 510(k) clearance on 1996-10-11, under 510(k) number K961368.

Who is the listed applicant for TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT?

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

What is the FDA product code for TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT?

The FDA product code for TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT is DPT.

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 Vasamedics, LLC 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: DPT)

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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