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IODOSORB POWDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870559
510(k) Type
Traditional
Applicant
PERSTORP AB C/O ROBERT JOEL SLOMOFF
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/20/1987
Days to Decision
38 days

IODOSORB POWDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870559
510(k) Type
Traditional
Applicant
PERSTORP AB C/O ROBERT JOEL SLOMOFF
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/20/1987
Days to Decision
38 days