Last synced on 25 April 2025 at 11:05 pm

PERTAC-HYBRID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900510
510(k) Type
Traditional
Applicant
ESPE GMBH (US)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1990
Days to Decision
188 days

PERTAC-HYBRID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900510
510(k) Type
Traditional
Applicant
ESPE GMBH (US)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1990
Days to Decision
188 days