Last synced on 23 September 2022 at 11:05 pm

BIOPSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820519
510(k) Type
Traditional
Applicant
ADVANCED BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
63 days

BIOPSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820519
510(k) Type
Traditional
Applicant
ADVANCED BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
63 days