CAPP TERMINAL DEVICE
FDA 510(k) clearance K780890 · decided 1978-06-13
Clearance details
- K-number
- K780890
- Device name
- CAPP TERMINAL DEVICE
- Applicant
- Hosmer Dorrance Corp.
- Decision
- Substantially Equivalent
- Date received
- 1978-05-31
- Decision date
- 1978-06-13
- Days to decision
- 13 days
- Clearance type
- Traditional
- Product code
- IQX
- Device class
- 1
- Regulation number
- 890.3420
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.