FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PURE WATER, INC.'S WATER PURIFICATION SYSTEMS

K Number: K992786 · Decision Jan 24, 2000
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
3
Review Days
158

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Basic Information

Device Name
PURE WATER, INC.'S WATER PURIFICATION SYSTEMS
K Number
K992786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pure Water, Inc.
Date Received
August 19, 1999
Decision Date
January 24, 2000
Product Code
FIP
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FIP Subsystem, Water Purification

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Other Clearances by Pure Water, Inc.

K Number Device Name
K993272 PURE WATER, INC.'S BICARB MIX, STORAGE AND DISTRIBUTION SYSTEM
K993058 PURE WATER INC'S ACIDIFIED STORAGE AND DISTRIBUTION SYSTEM WITH OPTIONAL REMOTE FILL