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REXTON PP 142, PP 142-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900636
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1990
Days to Decision
46 days

REXTON PP 142, PP 142-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900636
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1990
Days to Decision
46 days