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RH-801/GS MODEL TRANSQ(R)1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932621
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1994
Days to Decision
420 days
Submission Type
Summary

RH-801/GS MODEL TRANSQ(R)1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932621
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1994
Days to Decision
420 days
Submission Type
Summary