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FDA 510(k)

SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026

K-Number: K002427 · 2001-06-22

ApplicantSandhill Scientific, Inc.
Decision Date2001-06-22
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 is the device name listed in this FDA 510(k) record. The listed applicant is Sandhill Scientific, Inc.. It received FDA 510(k) clearance on 2001-06-22 under 510(k) number K002427. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026?

SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 is a medical device that received FDA 510(k) clearance on 2001-06-22. The listed applicant is Sandhill Scientific, Inc.. The 510(k) number is K002427.

When did SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 receive FDA 510(k) clearance?

SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 received FDA 510(k) clearance on 2001-06-22, under 510(k) number K002427.

Who is the listed applicant for SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026?

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

What is the FDA product code for SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026?

The FDA product code for SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 is FFX.

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Other records listing Sandhill Scientific, Inc. as applicant

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Related Devices (Code: FFX)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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