Last synced on 27 January 2023 at 11:04 pm

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880591
510(k) Type
Traditional
Applicant
LASER PERIPHERALS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1988
Days to Decision
111 days

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880591
510(k) Type
Traditional
Applicant
LASER PERIPHERALS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1988
Days to Decision
111 days