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FDA 510(k)

MODEL 110-5 & 140-8

K-Number: K842005 · 1984-08-03

ApplicantCamino Laboratories, Inc.
Decision Date1984-08-03
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 110-5 & 140-8 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 1984-08-03 under 510(k) number K842005. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 110-5 & 140-8?

MODEL 110-5 & 140-8 is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K842005.

When did MODEL 110-5 & 140-8 receive FDA 510(k) clearance?

MODEL 110-5 & 140-8 received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842005.

Who is the listed applicant for MODEL 110-5 & 140-8?

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 110-5 & 140-8?

The FDA product code for MODEL 110-5 & 140-8 is DXO.

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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: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, 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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