Last synced on 25 November 2022 at 11:04 pm

AUTOLINK BODY PLETHYSMOGRAPH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960121
510(k) Type
Traditional
Applicant
P.K. MORGAN LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
364 days
Submission Type
Statement

AUTOLINK BODY PLETHYSMOGRAPH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960121
510(k) Type
Traditional
Applicant
P.K. MORGAN LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
364 days
Submission Type
Statement