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FDA 510(k)

MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

K-Number: K893232 · 1989-07-14

ApplicantCamino Laboratories, Inc.
Decision Date1989-07-14
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM 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 1989-07-14 under 510(k) number K893232. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM?

MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K893232.

When did MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM receive FDA 510(k) clearance?

MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893232.

Who is the listed applicant for MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM?

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 MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM?

The FDA product code for MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM is DSK.

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Other records listing Camino Laboratories, 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.

K932769CAMINO VENTRICULAR DRAINAGE SYSTEMK930222CAMINO VENTRICULAR ACCESS DEVICEK930221CAMINO VENTRICULAR TRANSDUCER ACCESSORYK920088CAMINO VENTRICULAR NEEDLEK914735VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HMK912833CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY

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Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, Inc.

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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