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FDA 510(k)

CODMAN LUMBAR DRAINAGE CATHETER KIT

K-Number: K964923 · 1997-06-25

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1997-06-25
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN LUMBAR DRAINAGE CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1997-06-25 under 510(k) number K964923. 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 CODMAN LUMBAR DRAINAGE CATHETER KIT?

CODMAN LUMBAR DRAINAGE CATHETER KIT is a medical device that received FDA 510(k) clearance on 1997-06-25. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K964923.

When did CODMAN LUMBAR DRAINAGE CATHETER KIT receive FDA 510(k) clearance?

CODMAN LUMBAR DRAINAGE CATHETER KIT received FDA 510(k) clearance on 1997-06-25, under 510(k) number K964923.

Who is the listed applicant for CODMAN LUMBAR DRAINAGE CATHETER KIT?

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

What is the FDA product code for CODMAN LUMBAR DRAINAGE CATHETER KIT?

The FDA product code for CODMAN LUMBAR DRAINAGE CATHETER KIT is JXG.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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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.

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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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