SPECTROPHOTOMETER MODEL 650-40
FDA 510(k) clearance K790236 · decided 1979-03-15
Clearance details
- K-number
- K790236
- Device name
- SPECTROPHOTOMETER MODEL 650-40
- Applicant
- The Perkin-Elmer Corp.
- Decision
- Substantially Equivalent
- Date received
- 1979-02-01
- Decision date
- 1979-03-15
- Days to decision
- 42 days
- Clearance type
- Traditional
- Product code
- KHO
- Device class
- 1
- Regulation number
- 862.2560
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- 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.