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FDA 510(k)

VAN JON SUPER CLYSTER(KIT, ENEMA

K-Number: K843792 · 1985-04-22

ApplicantVan Jon Co.
Decision Date1985-04-22
Product CodeFCE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VAN JON SUPER CLYSTER(KIT, ENEMA is the device name listed in this FDA 510(k) record. The listed applicant is Van Jon Co.. It received FDA 510(k) clearance on 1985-04-22 under 510(k) number K843792. The device is classified under product code FCE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAN JON SUPER CLYSTER(KIT, ENEMA?

VAN JON SUPER CLYSTER(KIT, ENEMA is a medical device that received FDA 510(k) clearance on 1985-04-22. The listed applicant is Van Jon Co.. The 510(k) number is K843792.

When did VAN JON SUPER CLYSTER(KIT, ENEMA receive FDA 510(k) clearance?

VAN JON SUPER CLYSTER(KIT, ENEMA received FDA 510(k) clearance on 1985-04-22, under 510(k) number K843792.

Who is the listed applicant for VAN JON SUPER CLYSTER(KIT, ENEMA?

The FDA 510(k) record lists Van Jon Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAN JON SUPER CLYSTER(KIT, ENEMA?

The FDA product code for VAN JON SUPER CLYSTER(KIT, ENEMA is FCE.

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Related Devices (Code: FCE)

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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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