Last synced on 20 December 2024 at 11:05 pm

SPECULUM, VAGINAL, METAL FIBEROPTIC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864865
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1987
Days to Decision
29 days

SPECULUM, VAGINAL, METAL FIBEROPTIC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864865
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1987
Days to Decision
29 days