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PREEMICARE MODEL D1-X1, SERIES 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881476
510(k) Type
Traditional
Applicant
PREEMICARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
245 days

PREEMICARE MODEL D1-X1, SERIES 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881476
510(k) Type
Traditional
Applicant
PREEMICARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
245 days