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FDA 510(k)

CAMINO CSF DRAINAGE SYSTEM MODEL 040

K-Number: K861961 · 1986-08-12

Decision Date1986-08-12
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CAMINO CSF DRAINAGE SYSTEM MODEL 040 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 1986-08-12 under 510(k) number K861961. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMINO CSF DRAINAGE SYSTEM MODEL 040?

CAMINO CSF DRAINAGE SYSTEM MODEL 040 is a medical device that received FDA 510(k) clearance on 1986-08-12. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K861961.

When did CAMINO CSF DRAINAGE SYSTEM MODEL 040 receive FDA 510(k) clearance?

CAMINO CSF DRAINAGE SYSTEM MODEL 040 received FDA 510(k) clearance on 1986-08-12, under 510(k) number K861961.

Who is the listed applicant for CAMINO CSF DRAINAGE SYSTEM MODEL 040?

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 CSF DRAINAGE SYSTEM MODEL 040?

The FDA product code for CAMINO CSF DRAINAGE SYSTEM MODEL 040 is JXG.

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 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.

View all 18 devices →

Related Devices (Code: JXG)

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

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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