Last synced on 14 November 2025 at 11:06 pm

PHORESOR II,MODEL PM900

Page Type
Cleared 510(K)
510(k) Number
K982668
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1999
Days to Decision
214 days
Submission Type
Summary

PHORESOR II,MODEL PM900

Page Type
Cleared 510(K)
510(k) Number
K982668
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1999
Days to Decision
214 days
Submission Type
Summary