TERRY KERATOMETER— 510(k) K781650
Substantially EquivalentClifford M. Terry, M.C.
FDA 510(k) clearance K781650 for TERRY KERATOMETER, Substantially Equivalent on 1978-10-17. Applicant: Clifford M. Terry, M.C.. Device class: 1.
Clearance details
- Applicant
- Clifford M. Terry, M.C.
- Product code
- Code HJA
- Device class
- Class 1
- Regulation
- 21 CFR 886.1350
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code HJA
view allData sourced from openFDA. This site is unofficial and independent of the FDA.