Last synced on 23 May 2025 at 11:06 pm

PRISMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791297
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1979
Days to Decision
25 days

PRISMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791297
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1979
Days to Decision
25 days