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FDA 510(k)

INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT

K-Number: K902628 · 1991-02-25

ApplicantBiometric Research Institute, Inc.
Decision Date1991-02-25
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT is the device name listed in this FDA 510(k) record. The listed applicant is Biometric Research Institute, Inc.. It received FDA 510(k) clearance on 1991-02-25 under 510(k) number K902628. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT?

INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT is a medical device that received FDA 510(k) clearance on 1991-02-25. The listed applicant is Biometric Research Institute, Inc.. The 510(k) number is K902628.

When did INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT receive FDA 510(k) clearance?

INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT received FDA 510(k) clearance on 1991-02-25, under 510(k) number K902628.

Who is the listed applicant for INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT?

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

What is the FDA product code for INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT?

The FDA product code for INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT is DXG.

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 Biometric Research Institute, 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.

K902627INTERFLO MEDICAL MODEL OXI/CO FILA. THERMO. CATH.

Related Devices (Code: DXG)

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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