510(k) K760825
- Device
- Fungal Immunodiffusion Kit
- Applicant
- I M, INC.
- 510(k) number
- K760825
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-11-16
- Date received
- 1976-10-13
- 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