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EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020031
510(k) Type
Traditional
Applicant
NEOTHERMIA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2002
Days to Decision
82 days
Submission Type
Summary