Last synced on 2 December 2022 at 11:04 pm

GEREONICS ULTRA-PIEZO RESPIRATORY EFFORT SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991411
510(k) Type
Traditional
Applicant
GEREONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1999
Days to Decision
33 days
Submission Type
Statement

GEREONICS ULTRA-PIEZO RESPIRATORY EFFORT SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991411
510(k) Type
Traditional
Applicant
GEREONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1999
Days to Decision
33 days
Submission Type
Statement