510(k) K761337
- Device
- AQUAMATIC K-MODULE MODEL K-10
- Applicant
- Gorman Rupp Industries
- 510(k) number
- K761337
- Product code
- JRR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-01-10
- Date received
- 1976-12-27
- Regulation
- 862.2050
- Classification name
- Regulator, Temperature
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3002889627
- 3043088937
- 3006421415
- 1424489
- 3009420598
- 3015967359
- 3043138885
- 3027645317
- 3035708936
- 3007456622
Source Documents#
510(k) summary PDF not indicated by FDA