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FDA 510(k)

COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/)

K-Number: K962928 · 1996-12-20

Decision Date1996-12-20
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) is the device name listed in this FDA 510(k) record. The listed applicant is Camino Neurocare, Inc.. It received FDA 510(k) clearance on 1996-12-20 under 510(k) number K962928. 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 COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/)?

COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) is a medical device that received FDA 510(k) clearance on 1996-12-20. The listed applicant is Camino Neurocare, Inc.. The 510(k) number is K962928.

When did COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) receive FDA 510(k) clearance?

COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) received FDA 510(k) clearance on 1996-12-20, under 510(k) number K962928.

Who is the listed applicant for COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/)?

The FDA 510(k) record lists Camino Neurocare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/)?

The FDA product code for COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/) is GWM.

Related Clinical Trials

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.

Other records listing Camino Neurocare, 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.

Related Devices (Code: GWM)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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