INTRAVENOUS START KIT
FDA 510(k) clearance K843813 · decided 1984-12-05
Clearance details
- K-number
- K843813
- Device name
- INTRAVENOUS START KIT
- Applicant
- Pro-Lab, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-09-28
- Decision date
- 1984-12-05
- Days to decision
- 68 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Round Rock, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.