FDA 510(k)

SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS

K-Number: K894300 · 1990-03-13

ApplicantU.S. Filter/Continental Water Systems

Decision Date1990-03-13

Product CodeFIP

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Filter/Continental Water Systems. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K894300. 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 SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS?

SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is U.S. Filter/Continental Water Systems. The 510(k) number is K894300.

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

SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS received FDA 510(k) clearance on 1990-03-13, under 510(k) number K894300.

Who is the listed applicant for SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS?

The FDA 510(k) record lists U.S. Filter/Continental Water Systems as the applicant. This does not by itself establish the device manufacturer.

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

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

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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.