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FDA 510(k)

SIPHONGUARD CSF CONTROL DEVICE

K-Number: K992173 · 2000-04-07

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date2000-04-07
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIPHONGUARD CSF CONTROL DEVICE 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 2000-04-07 under 510(k) number K992173. 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 SIPHONGUARD CSF CONTROL DEVICE?

SIPHONGUARD CSF CONTROL DEVICE is a medical device that received FDA 510(k) clearance on 2000-04-07. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K992173.

When did SIPHONGUARD CSF CONTROL DEVICE receive FDA 510(k) clearance?

SIPHONGUARD CSF CONTROL DEVICE received FDA 510(k) clearance on 2000-04-07, under 510(k) number K992173.

Who is the listed applicant for SIPHONGUARD CSF CONTROL DEVICE?

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 SIPHONGUARD CSF CONTROL DEVICE?

The FDA product code for SIPHONGUARD CSF CONTROL DEVICE is JXG.

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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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