RETIC-SET
FDA 510(k) clearance K841848 · decided 1984-05-31
Clearance details
- K-number
- K841848
- Device name
- RETIC-SET
- Applicant
- R&D Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-03-28
- Decision date
- 1984-05-31
- Days to decision
- 64 days
- Clearance type
- Traditional
- Product code
- KQC
- Device class
- 1
- Regulation number
- 864.1850
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch R&D Systems
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| FIELDTEX HEMATOXYLIN (K882873) | Anatech, Ltd. | 1988-07-28 |
| GENERAL DIAGNOSTICS COAG-A-MATE XC (K852843) | Warner-Lambert Co. | 1985-08-13 |
| RETIC-SET (K843619) | R&D Systems, Inc. | 1984-10-30 |
| PONCEAU S STAIN SET (K792550) | Electrophoresis Corp. of America | 1980-01-16 |
| VOLU-SOL NMB RETICULOCYTE STAIN (K792496) | Volu Sol Medical Industries | 1979-12-31 |
| STAT DIFF STAIN (K791007) | Bioscientific | 1979-08-03 |
| HEMASTAIN FIXATIVE (K760485) | Geometric Data, Div. Smithkline Corp. | 1976-08-30 |
| HEMASTAIN PHOSPHATE BUFFER (K760487) | Geometric Data, Div. Smithkline Corp. | 1976-08-30 |
Recalls involving this device
No recalls on record reference this clearance.