Last synced on 20 June 2025 at 11:06 pm

LIGHTSPEED DENTAL HAND INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932529
510(k) Type
Traditional
Applicant
LIGHTSPEED ENDODONTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1993
Days to Decision
163 days
Submission Type
Statement

LIGHTSPEED DENTAL HAND INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932529
510(k) Type
Traditional
Applicant
LIGHTSPEED ENDODONTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1993
Days to Decision
163 days
Submission Type
Statement