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BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981246
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1999
Days to Decision
415 days
Submission Type
Statement

BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981246
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1999
Days to Decision
415 days
Submission Type
Statement