ACU-ALERT
FDA 510(k) clearance K791399 · decided 1979-10-11
Clearance details
- K-number
- K791399
- Device name
- ACU-ALERT
- Applicant
- Acumed Instruments Corp.
- Decision
- Substantially Equivalent
- Date received
- 1979-07-16
- Decision date
- 1979-10-11
- Days to decision
- 87 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.