Last synced on 19 July 2024 at 11:05 pm

NAGASHIMA F60MM ATTACH. LENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821705
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1982
Days to Decision
30 days

NAGASHIMA F60MM ATTACH. LENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821705
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1982
Days to Decision
30 days