FDA 510(k)

CAMINO VENTRICULAR TRANSDUCER ACCESSORY

K-Number: K930221 · 1993-04-15

Decision Date1993-04-15

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CAMINO VENTRICULAR TRANSDUCER ACCESSORY 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 1993-04-15 under 510(k) number K930221. 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 CAMINO VENTRICULAR TRANSDUCER ACCESSORY?

CAMINO VENTRICULAR TRANSDUCER ACCESSORY is a medical device that received FDA 510(k) clearance on 1993-04-15. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K930221.

When did CAMINO VENTRICULAR TRANSDUCER ACCESSORY receive FDA 510(k) clearance?

CAMINO VENTRICULAR TRANSDUCER ACCESSORY received FDA 510(k) clearance on 1993-04-15, under 510(k) number K930221.

Who is the listed applicant for CAMINO VENTRICULAR TRANSDUCER ACCESSORY?

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 CAMINO VENTRICULAR TRANSDUCER ACCESSORY?

The FDA product code for CAMINO VENTRICULAR TRANSDUCER ACCESSORY is GWM.

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Other records listing Camino Laboratories, Inc. as applicant

K932769CAMINO VENTRICULAR DRAINAGE SYSTEM K930222CAMINO VENTRICULAR ACCESS DEVICE K920088CAMINO VENTRICULAR NEEDLE K914735VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM K912833CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY K893232MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

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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.