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SPATULA FOR PAP SMEAR COLLECTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893229
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1990
Days to Decision
300 days

SPATULA FOR PAP SMEAR COLLECTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893229
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1990
Days to Decision
300 days