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FDA 510(k)

MISHLER 2 CHAMB FLUSHING VALVE,STAND

K-Number: K760784 · 1976-11-01

ApplicantHeyer Schulte Corp.
Decision Date1976-11-01
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MISHLER 2 CHAMB FLUSHING VALVE,STAND 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 1976-11-01 under 510(k) number K760784. 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 MISHLER 2 CHAMB FLUSHING VALVE,STAND?

MISHLER 2 CHAMB FLUSHING VALVE,STAND is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Heyer Schulte Corp.. The 510(k) number is K760784.

When did MISHLER 2 CHAMB FLUSHING VALVE,STAND receive FDA 510(k) clearance?

MISHLER 2 CHAMB FLUSHING VALVE,STAND received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760784.

Who is the listed applicant for MISHLER 2 CHAMB FLUSHING VALVE,STAND?

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 MISHLER 2 CHAMB FLUSHING VALVE,STAND?

The FDA product code for MISHLER 2 CHAMB FLUSHING VALVE,STAND is JXG.

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Other records listing Heyer Schulte Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K7920962 FR KELMAN CHAMBER MAINTAINERK790842SUBCUTANEOUS TISSUE EXPANDERK780706LUMBAR NERVE ROOT SHIELDK780417ASEPTIC TRANSFER SETK771224RADOVAN SUBCUTANEOUS TISSUE EXPANDERK760778T-TUBE DRAIN, ROUND

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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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