'NO-BOIL' FOLIC ACID KIT
FDA 510(k) clearance K810003 · decided 1981-01-21
Clearance details
- K-number
- K810003
- Device name
- 'NO-BOIL' FOLIC ACID KIT
- Applicant
- Diagnostic Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1981-01-06
- Decision date
- 1981-01-21
- Days to decision
- 15 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.