BLOOD ADMINISTRATION SET
FDA 510(k) clearance K920788 · decided 1992-06-04
Clearance details
- K-number
- K920788
- Device name
- BLOOD ADMINISTRATION SET
- Applicant
- Douglas Medical Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1992-02-20
- Decision date
- 1992-06-04
- Days to decision
- 105 days
- Clearance type
- Traditional
- Product code
- BRZ
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Mundelein, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.