Last synced on 23 February 2024 at 11:04 pm

CLASS II DEVICE FOR I.C.P. MONITORING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822636
510(k) Type
Traditional
Applicant
PHILADELPHIA MEDICAL SPECIALTIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
14 days

CLASS II DEVICE FOR I.C.P. MONITORING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822636
510(k) Type
Traditional
Applicant
PHILADELPHIA MEDICAL SPECIALTIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
14 days