Last synced on 7 June 2024 at 11:04 pm

SIPHONGUARD CSF CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992173
510(k) Type
Traditional
Applicant
JOHNSON & JOHNSON PROFESSIONALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2000
Days to Decision
284 days
Submission Type
Summary

SIPHONGUARD CSF CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992173
510(k) Type
Traditional
Applicant
JOHNSON & JOHNSON PROFESSIONALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2000
Days to Decision
284 days
Submission Type
Summary