510(k) K760066
- Device
- Tray, Iced Injectable (26420)
- Applicant
- INSTRUMENTATION LABORATORY CO.
- 510(k) number
- K760066
- Product code
- DXL
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-07-21
- Date received
- 1976-06-16
- Regulation
- 870.1660
- Classification name
- Injector, Indicator
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Related Records
Applicant Contact
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents
510(k) summary PDF not indicated by FDA