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FDA 510(k)

VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH.

K-Number: K760502 · 1976-08-30

ApplicantJoe W. Utt
Decision Date1976-08-30
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. is the device name listed in this FDA 510(k) record. The listed applicant is Joe W. Utt. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760502. 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 VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH.?

VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Joe W. Utt. The 510(k) number is K760502.

When did VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. receive FDA 510(k) clearance?

VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760502.

Who is the listed applicant for VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH.?

The FDA 510(k) record lists Joe W. Utt as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH.?

The FDA product code for VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. is JXG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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