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FDA 510(k)

CAMINO VENTRICULAR NEEDLE

K-Number: K920088 · 1992-05-01

ApplicantCamino Laboratories, Inc.
Decision Date1992-05-01
Product CodeHCD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CAMINO VENTRICULAR NEEDLE 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 1992-05-01 under 510(k) number K920088. The device is classified under product code HCD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMINO VENTRICULAR NEEDLE?

CAMINO VENTRICULAR NEEDLE is a medical device that received FDA 510(k) clearance on 1992-05-01. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K920088.

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

CAMINO VENTRICULAR NEEDLE received FDA 510(k) clearance on 1992-05-01, under 510(k) number K920088.

Who is the listed applicant for CAMINO VENTRICULAR NEEDLE?

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 NEEDLE?

The FDA product code for CAMINO VENTRICULAR NEEDLE is HCD.

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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 ACCESSORYK914735VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HMK912833CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAYK893232MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

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Related Devices (Code: HCD)

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.

K102101SURGIVISION MR COMPATIBLE VENTRICULAR CANNULASurgivision, 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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