FDA Browser

Last synced on 18 April 2025 at 11:05 pm

subpart-f—therapeutic-devices/

PROMED 55-G SOFT DAILY WEAR CONTACT LENS

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K970615
510(k) Type: Traditional
Applicant: BIOMED DEVICES CORP.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 3/19/1997
Days to Decision: 29 days
Submission Type: Statement

FDA Browser

subpart-f—therapeutic-devices/

PROMED 55-G SOFT DAILY WEAR CONTACT LENS

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K970615
510(k) Type: Traditional
Applicant: BIOMED DEVICES CORP.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 3/19/1997
Days to Decision: 29 days
Submission Type: Statement