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FDA 510(k)

REVERSE OSMOSIS WATER PURIFICATION SYSTEM

K-Number: K871242 · 1988-03-16

ApplicantMedro Systems, Inc.
Decision Date1988-03-16
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REVERSE OSMOSIS WATER PURIFICATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medro Systems, Inc.. It received FDA 510(k) clearance on 1988-03-16 under 510(k) number K871242. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVERSE OSMOSIS WATER PURIFICATION SYSTEM?

REVERSE OSMOSIS WATER PURIFICATION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-16. The listed applicant is Medro Systems, Inc.. The 510(k) number is K871242.

When did REVERSE OSMOSIS WATER PURIFICATION SYSTEM receive FDA 510(k) clearance?

REVERSE OSMOSIS WATER PURIFICATION SYSTEM received FDA 510(k) clearance on 1988-03-16, under 510(k) number K871242.

Who is the listed applicant for REVERSE OSMOSIS WATER PURIFICATION SYSTEM?

The FDA 510(k) record lists Medro Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REVERSE OSMOSIS WATER PURIFICATION SYSTEM?

The FDA product code for REVERSE OSMOSIS WATER PURIFICATION SYSTEM is FIP.

Related Clinical Trials

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Related Devices (Code: FIP)

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.

K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLCK251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLCK252181AquaAFresenius Medical Care North AmericaK250514UPT Series Medical RO Water Treatment SystemSpecialty Water Technologies, Inc.K232953AquaBplus; AquaB LITEFresenius Medical Care Renal Therapies Group, LLCK223479AQUAbase nXB.Braun Medical, Inc.

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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