510(k) K841652
- Device
- Ocular Pressure Applicator
- Applicant
- THE LEBANON CORP.
- 510(k) number
- K841652
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-06-01
- Date received
- 1984-04-20
- Review panel
- Unknown
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents#
510(k) summary PDF not indicated by FDA