Last synced on 25 April 2025 at 11:05 pm

ARAMIS II DERMATOLOGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032260
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
121 days
Submission Type
Summary

ARAMIS II DERMATOLOGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032260
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
121 days
Submission Type
Summary