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FDA 510(k)

DIAMOND II VALVE

K-Number: K991429 · 1999-05-19

ApplicantPhoenix Biomedical Corp.
Decision Date1999-05-19
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIAMOND II VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Biomedical Corp.. It received FDA 510(k) clearance on 1999-05-19 under 510(k) number K991429. 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 DIAMOND II VALVE?

DIAMOND II VALVE is a medical device that received FDA 510(k) clearance on 1999-05-19. The listed applicant is Phoenix Biomedical Corp.. The 510(k) number is K991429.

When did DIAMOND II VALVE receive FDA 510(k) clearance?

DIAMOND II VALVE received FDA 510(k) clearance on 1999-05-19, under 510(k) number K991429.

Who is the listed applicant for DIAMOND II VALVE?

The FDA 510(k) record lists Phoenix Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAMOND II VALVE?

The FDA product code for DIAMOND II VALVE is JXG.

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Other records listing Phoenix Biomedical Corp. as applicant

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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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