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FDA 510(k)

TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER

K-Number: K881303 · 1988-11-29

ApplicantTriton Technology, Inc.
Decision Date1988-11-29
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Triton Technology, Inc.. It received FDA 510(k) clearance on 1988-11-29 under 510(k) number K881303. 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 TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER?

TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER is a medical device that received FDA 510(k) clearance on 1988-11-29. The listed applicant is Triton Technology, Inc.. The 510(k) number is K881303.

When did TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER receive FDA 510(k) clearance?

TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER received FDA 510(k) clearance on 1988-11-29, under 510(k) number K881303.

Who is the listed applicant for TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER?

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

What is the FDA product code for TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER?

The FDA product code for TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER is DPT.

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Other records listing Triton Technology, Inc. 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.

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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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