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ROPE SYSTEM REVERSE OSMOSIS PERITONEAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844630
510(k) Type
Traditional
Applicant
ORGANON TEKNIKA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1985
Days to Decision
105 days

ROPE SYSTEM REVERSE OSMOSIS PERITONEAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844630
510(k) Type
Traditional
Applicant
ORGANON TEKNIKA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1985
Days to Decision
105 days