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FDA 510(k)

DP240 240 HOUR DOPPLER PROBE

K-Number: K052989 · 2006-03-08

Decision Date2006-03-08
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DP240 240 HOUR DOPPLER PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Deltex Medical. It received FDA 510(k) clearance on 2006-03-08 under 510(k) number K052989. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DP240 240 HOUR DOPPLER PROBE?

DP240 240 HOUR DOPPLER PROBE is a medical device that received FDA 510(k) clearance on 2006-03-08. The listed applicant is Deltex Medical. The 510(k) number is K052989.

When did DP240 240 HOUR DOPPLER PROBE receive FDA 510(k) clearance?

DP240 240 HOUR DOPPLER PROBE received FDA 510(k) clearance on 2006-03-08, under 510(k) number K052989.

Who is the listed applicant for DP240 240 HOUR DOPPLER PROBE?

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

What is the FDA product code for DP240 240 HOUR DOPPLER PROBE?

The FDA product code for DP240 240 HOUR DOPPLER PROBE 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 Deltex Medical 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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