DIA-H 1/2/3 & DIA-HT 1/2/3
FDA 510(k) clearance K840801 · decided 1984-04-25
Clearance details
- K-number
- K840801
- Device name
- DIA-H 1/2/3 & DIA-HT 1/2/3
- Applicant
- Diatech, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-02-23
- Decision date
- 1984-04-25
- Days to decision
- 62 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.