FDA 510(k)

VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM

K-Number: K914735 · 1992-01-17

Decision Date1992-01-17

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM is the device name listed in this FDA 510(k) record. The listed applicant is Camino Laboratories, Inc.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K914735. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM?

VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K914735.

When did VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM receive FDA 510(k) clearance?

VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM received FDA 510(k) clearance on 1992-01-17, under 510(k) number K914735.

Who is the listed applicant for VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM?

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

What is the FDA product code for VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM?

The FDA product code for VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM is GWM.

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Other records listing Camino Laboratories, Inc. as applicant

K932769CAMINO VENTRICULAR DRAINAGE SYSTEM K930222CAMINO VENTRICULAR ACCESS DEVICE K930221CAMINO VENTRICULAR TRANSDUCER ACCESSORY K920088CAMINO VENTRICULAR NEEDLE K912833CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY K893232MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

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Related Devices (Code: GWM)

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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.