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FDA 510(k)

VALVE, STANDARD MODEL PUDENZE FLUSHING

K-Number: K760501 · 1976-08-30

ApplicantHeyer Schulte Corp.
Decision Date1976-08-30
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VALVE, STANDARD MODEL PUDENZE FLUSHING is the device name listed in this FDA 510(k) record. The listed applicant is Heyer Schulte Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760501. 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, STANDARD MODEL PUDENZE FLUSHING?

VALVE, STANDARD MODEL PUDENZE FLUSHING is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Heyer Schulte Corp.. The 510(k) number is K760501.

When did VALVE, STANDARD MODEL PUDENZE FLUSHING receive FDA 510(k) clearance?

VALVE, STANDARD MODEL PUDENZE FLUSHING received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760501.

Who is the listed applicant for VALVE, STANDARD MODEL PUDENZE FLUSHING?

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

What is the FDA product code for VALVE, STANDARD MODEL PUDENZE FLUSHING?

The FDA product code for VALVE, STANDARD MODEL PUDENZE FLUSHING is JXG.

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Other records listing Heyer Schulte 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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