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FDA 510(k)

PHYSIOLOGICAL PRESS. MEASUREMENT CATH

K-Number: K832579 · 1983-10-20

ApplicantCamino Laboratories, Inc.
Decision Date1983-10-20
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL PRESS. MEASUREMENT CATH 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 1983-10-20 under 510(k) number K832579. 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 PHYSIOLOGICAL PRESS. MEASUREMENT CATH?

PHYSIOLOGICAL PRESS. MEASUREMENT CATH is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K832579.

When did PHYSIOLOGICAL PRESS. MEASUREMENT CATH receive FDA 510(k) clearance?

PHYSIOLOGICAL PRESS. MEASUREMENT CATH received FDA 510(k) clearance on 1983-10-20, under 510(k) number K832579.

Who is the listed applicant for PHYSIOLOGICAL PRESS. MEASUREMENT CATH?

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 PHYSIOLOGICAL PRESS. MEASUREMENT CATH?

The FDA product code for PHYSIOLOGICAL PRESS. MEASUREMENT CATH 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 SYSTEMK930221CAMINO VENTRICULAR TRANSDUCER ACCESSORYK930222CAMINO VENTRICULAR ACCESS DEVICEK920088CAMINO 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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