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3M MULTI-ALLERGEN IGE FASTSCREEN(TM) S8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900244
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1990
Days to Decision
35 days

3M MULTI-ALLERGEN IGE FASTSCREEN(TM) S8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900244
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1990
Days to Decision
35 days