Last synced on 18 April 2025 at 11:05 pm

ASAP ARTHROSCOPE MODELS; 10-0001-00, 10-0002-00, 10-0003-00, 10-0004-00, 10-0005-00, 10-0006-00, 10-0007-00, 10-0008-00,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031972
510(k) Type
Traditional
Applicant
ASAP ENDOSCOPIC PRODUCTS GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/15/2003
Days to Decision
81 days
Submission Type
Summary

ASAP ARTHROSCOPE MODELS; 10-0001-00, 10-0002-00, 10-0003-00, 10-0004-00, 10-0005-00, 10-0006-00, 10-0007-00, 10-0008-00,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031972
510(k) Type
Traditional
Applicant
ASAP ENDOSCOPIC PRODUCTS GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/15/2003
Days to Decision
81 days
Submission Type
Summary