Last synced on 9 May 2025 at 11:05 pm

AUTOWAND(TM) 7XXX SERIES, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904888
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1991
Days to Decision
82 days

AUTOWAND(TM) 7XXX SERIES, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904888
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1991
Days to Decision
82 days