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FDA 510(k)

MAINSTREAM WATER PURIFICATION DEVICE

K-Number: K012716 · 2002-05-07

ApplicantPrismedical Corp.
Decision Date2002-05-07
Product CodeNHV
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAINSTREAM WATER PURIFICATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Prismedical Corp.. It received FDA 510(k) clearance on 2002-05-07 under 510(k) number K012716. The device is classified under product code NHV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAINSTREAM WATER PURIFICATION DEVICE?

MAINSTREAM WATER PURIFICATION DEVICE is a medical device that received FDA 510(k) clearance on 2002-05-07. The listed applicant is Prismedical Corp.. The 510(k) number is K012716.

When did MAINSTREAM WATER PURIFICATION DEVICE receive FDA 510(k) clearance?

MAINSTREAM WATER PURIFICATION DEVICE received FDA 510(k) clearance on 2002-05-07, under 510(k) number K012716.

Who is the listed applicant for MAINSTREAM WATER PURIFICATION DEVICE?

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

What is the FDA product code for MAINSTREAM WATER PURIFICATION DEVICE?

The FDA product code for MAINSTREAM WATER PURIFICATION DEVICE is NHV.

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Related Devices (Code: NHV)

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.

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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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