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PHORESOR II, MODEL PM900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974855
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/27/1998
Days to Decision
88 days

PHORESOR II, MODEL PM900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974855
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/27/1998
Days to Decision
88 days