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GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971920
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1997
Days to Decision
195 days
Submission Type
Statement

GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971920
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1997
Days to Decision
195 days
Submission Type
Statement