CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR
FDA 510(k) clearance K760072 · decided 1976-07-20
Clearance details
- K-number
- K760072
- Device name
- CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR
- Applicant
- Bemis Health Care
- Decision
- Substantially Equivalent
- Date received
- 1976-06-18
- Decision date
- 1976-07-20
- Days to decision
- 32 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- 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.