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ULTRA-KLEEN POWDER FOR DENTAL UNIT WATER LINES, MODELS 513P, 505L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991946
510(k) Type
Traditional
Applicant
STERILEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1999
Days to Decision
86 days
Submission Type
Statement

ULTRA-KLEEN POWDER FOR DENTAL UNIT WATER LINES, MODELS 513P, 505L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991946
510(k) Type
Traditional
Applicant
STERILEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1999
Days to Decision
86 days
Submission Type
Statement