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FDA 510(k)

REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION

K-Number: K931595 · 1994-12-29

ApplicantOsmonics, Inc.
Decision Date1994-12-29
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Osmonics, Inc.. It received FDA 510(k) clearance on 1994-12-29 under 510(k) number K931595. 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 EQUIPMENT FOR WATER PURIFICATION?

REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Osmonics, Inc.. The 510(k) number is K931595.

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

REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION received FDA 510(k) clearance on 1994-12-29, under 510(k) number K931595.

Who is the listed applicant for REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION?

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

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

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

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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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