THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE
FDA 510(k) clearance K827748 · decided 1982-08-16
Clearance details
- K-number
- K827748
- Device name
- THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE
- Applicant
- Kemble Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-07-20
- Decision date
- 1982-08-16
- Days to decision
- 27 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Raleigh, NC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.