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FDA 510(k)

CODMAN HAKIM MICRO PRECISION VALVE

K-Number: K973774 · 1997-12-29

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1997-12-29
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN HAKIM MICRO PRECISION VALVE 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 1997-12-29 under 510(k) number K973774. 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 HAKIM MICRO PRECISION VALVE?

CODMAN HAKIM MICRO PRECISION VALVE is a medical device that received FDA 510(k) clearance on 1997-12-29. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K973774.

When did CODMAN HAKIM MICRO PRECISION VALVE receive FDA 510(k) clearance?

CODMAN HAKIM MICRO PRECISION VALVE received FDA 510(k) clearance on 1997-12-29, under 510(k) number K973774.

Who is the listed applicant for CODMAN HAKIM MICRO PRECISION VALVE?

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 HAKIM MICRO PRECISION VALVE?

The FDA product code for CODMAN HAKIM MICRO PRECISION VALVE is JXG.

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Related Devices (Code: 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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