DAKO PAP KIT K509
FDA 510(k) clearance K820336 · decided 1982-07-13
Clearance details
- K-number
- K820336
- Device name
- DAKO PAP KIT K509
- Applicant
- Dako Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-02-08
- Decision date
- 1982-07-13
- Days to decision
- 155 days
- Clearance type
- Traditional
- Product code
- LIJ
- Device class
- 1
- Regulation number
- 864.4400
- Medical specialty
- Pathology
- Advisory committee
- Pathology
- 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 |
|---|---|---|
| AMERICAN HISTO-ID SYS PRIMARY KIT PSA PROSTATE ANT (K855034) | Bartels Immunodiagnostic Supplies, Inc. | 1986-03-11 |
Recalls involving this device
No recalls on record reference this clearance.