BLUE RIDGE RABBIT BLOOD
FDA 510(k) clearance K820849 · decided 1982-04-16
Clearance details
- K-number
- K820849
- Device name
- BLUE RIDGE RABBIT BLOOD
- Applicant
- Blue Ridge Media Co.
- Decision
- Substantially Equivalent
- Date received
- 1982-03-26
- Decision date
- 1982-04-16
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- LHW
- Device class
- 1
- Regulation number
- 866.3720
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| BLUE RIDGE SHEEP BLOOD (K820848) | Blue Ridge Media Co. | 1982-04-16 |
| AFRICAN GREEN MONKEY BLOOD IN ALSERVERS (K813513) | Dutchland Laboratories, Inc. | 1981-12-31 |
| RHESUS MONKEY BLOOD IN ALSEVER'S (K813512) | Dutchland Laboratories, Inc. | 1981-12-29 |
Recalls involving this device
No recalls on record reference this clearance.