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OMICRON MONITOR, DELTA MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960861
510(k) Type
Traditional
Applicant
CORE-M, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/19/1996
Days to Decision
171 days

OMICRON MONITOR, DELTA MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960861
510(k) Type
Traditional
Applicant
CORE-M, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/19/1996
Days to Decision
171 days