510(k) K771371
- Device
- SCREENING COMPUTEO SC-20
- Applicant
- Cavitron Corp.
- 510(k) number
- K771371
- Product code
- BZM
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-08-04
- Date received
- 1977-07-25
- Regulation
- 868.1900
- Classification name
- Calculator, Pulmonary Function Interpretor (Diagnostic)
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 2183022
- 2023529
Source Documents#
510(k) summary PDF not indicated by FDA
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