FDA 510(k)

VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H

K-Number: K881183 · 1988-05-04

Decision Date1988-05-04

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H 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 1988-05-04 under 510(k) number K881183. 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 BOLT PRESSURE MONITORING KIT #110-4H?

VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H is a medical device that received FDA 510(k) clearance on 1988-05-04. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K881183.

When did VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H receive FDA 510(k) clearance?

VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H received FDA 510(k) clearance on 1988-05-04, under 510(k) number K881183.

Who is the listed applicant for VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H?

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 BOLT PRESSURE MONITORING KIT #110-4H?

The FDA product code for VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H 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 K914735VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM K912833CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY

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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.