CELL
FDA 510(k) clearance K780305 · decided 1978-03-27
Clearance details
- K-number
- K780305
- Device name
- CELL
- Applicant
- Dynatech Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1978-02-23
- Decision date
- 1978-03-27
- Days to decision
- 32 days
- Clearance type
- Traditional
- Product code
- KJF
- Device class
- 1
- Regulation number
- 864.2240
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- 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 |
|---|---|---|
| LIFECELL RECOVERY CONTAINER (K893787) | Baxter Healthcare Corp | 1989-06-23 |
| AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY (K892645) | Amicon, Inc. | 1989-06-13 |
| TOOTH PRESERVING SYSTEM (K875221) | Biological Rescue Products, Inc. | 1988-04-14 |
Recalls involving this device
No recalls on record reference this clearance.